Klor-con M label

Klor-con M

Klor-con M Recall

Get an alert when a recall is issued.

Side Effects & Adverse Reactions

Liver warning: This product contains acetaminophen. The maximum daily dose of this product is 10 caplets (3,250 mg acetaminophen) in 24 hours. Severe liver damage may occur if you take:

  • more than 4,000 mg of acetaminophen in 24 hours
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product
Do not use

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

  • if you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

  • liver disease
  • thyroid disease
  • diabetes
  • heart disease
  • high blood pressure
  • trouble urinating due to enlarged prostate gland 
Ask a doctor or pharmacist before use if you are

taking the blood thinning drug warfarin.

When using this product

do not exceed recommended dosage.

Stop use and ask a doctor if

  • nervousness, dizziness, or sleeplessness occur
  • pain or nasal congestion gets worse or lasts more than 7 days
  • new symptoms occur
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present

These could be signs of a serious condition.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

Overdose warning: Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Do not use

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

  • if you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

  • liver disease
  • thyroid disease
  • diabetes
  • heart disease
  • high blood pressure
  • trouble urinating due to enlarged prostate gland 

Ask a doctor or pharmacist before use if you are

taking the blood thinning drug warfarin.

Stop use and ask a doctor if

  • nervousness, dizziness, or sleeplessness occur
  • pain or nasal congestion gets worse or lasts more than 7 days
  • new symptoms occur
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present

These could be signs of a serious condition.

FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.

Uses

  • temporarily relieves these symptoms associated with hay fever or other respiratory allergies, and the common cold:
    • headache
    • nasal congestion
    • minor aches and pains
    • sinus congestion and pressure
  • helps decongest sinus openings and passages
  • promotes sinus drainage
  • helps clear nasal passages
  • temporarily reduces fever

History

There is currently no drug history available for this drug.

Other Information

There are no additional details available for this product.

Klor-con M Manufacturers

  • Klor-con M | Salado Sales, Inc.
    No Recall

    Klor-con M | Salado Sales, Inc.

    Klor-con M | Salado Sales, Inc.
    do not take more than directed (see overdose warning) adults and children 12 years and over take 2 caplets every 4 hours swallow whole - do not crush, chew, or dissolve do not take more than 10 caplets in 24 hours children under 12 years: ask a doctor
  • Ncs Healthcare Of Ky, Inc Dba Vangard Labs
    Klor-con M | Appco Pharmaceuticals Corp
    No Recall

    Klor-con M | Appco Pharmaceuticals Corp

    Klor-con M | Appco Pharmaceuticals Corp

    Trichomoniasis

    In the Female
    One-day treatment - two grams of METRONIDAZOLE, USP given either as a single dose or in two divided doses of one gram each, given in the same day.

    Seven-day course of treatment - 250 mg three times daily for seven consecutive days. There is some indication from controlled comparative studies that cure rates as determined by vaginal smears and signs and symptoms, may be higher after a seven-day course of treatment than after a one-day treatment regimen.

    The dosage regimen should be individualized. Single-dose treatment can assure compliance, especially if administered under supervision, in those patients who cannot be relied on to continue the seven-day regimen. A seven-day course of treatment may minimize reinfection by protecting the patient long enough for the sexual contacts to obtain appropriate treatment. Further, some patients may tolerate one treatment regimen better than the other.

    Pregnant patients should not be treated during the first trimester (see CONTRAINDICATIONS). In pregnant patients for whom alternative treatment has been inadequate, the one-day course of therapy should not be used, as it results in higher serum levels which can reach the fetal circulation (see PRECAUTIONS-Pregnancy).

    When repeat courses of the drug are required, it is recommended that an interval of four to six weeks elapse between courses and that the presence of the trichomonad be reconfirmed by appropriate laboratory measures. Total and differential leukocyte counts should be made before and after re-treatment.

    In the Male: Treatment should be individualized as it is for the female.

    Amebiasis

    Adults:
    For acute intestinal amebiasis (acute amebic dysentery):750 mg orally three times daily for 5 to 10 days.

    For amebic liver abscess:500 mg or 750 mg orally three times daily for 5 to 10 days.

    Pediatric patients: 35 to 50 mg/kg/24 hours, divided into three doses, orally for 10 days.

    Anaerobic Bacterial Infections

    In the treatment of most serious anaerobic infections, intravenous metronidazole is usually administered initially.

    The usual adult oral dosage is 7.5 mg/kg every six hours (approx. 500 mg for a 70-kg adult). A maximum of 4 g should not be exceeded during a 24-hour period.

    The usual duration of therapy is 7 to 10 days; however, infections of the bone and joint, lower respiratory tract, and endocardium may require longer treatment.

    Dosage Adjustment

    Patients with Severe Hepatic Impairment

    For patients with severe hepatic impairment (Child-Pugh C), the dose of METRONIDAZOLE, USP should be reduced by 50% (see CLINICAL PHARMACOLOGY and PRECAUTIONS).

    Patients Undergoing Hemodialysis:

    Hemodialysis removes significant amounts of metronidazole and its metabolites from systemic circulation. The clearance of metronidazole will depend on the type of dialysis membrane used, the duration of the dialysis session, and other factors. If the administration of metronidazole cannot be separated from the hemodialysis session, supplementation of metronidazole dosage following the hemodialysis session should be considered, depending on the patient’s clinical situation (see CLINICAL PHARMACOLOGY).

    Dosage Adjustment

    Patients with Severe Hepatic Impairment

    For patients with severe hepatic impairment (Child-Pugh C), the dose of METRONIDAZOLE, USP should be reduced by 50% (see CLINICAL PHARMACOLOGY and PRECAUTIONS).

    Patients Undergoing Hemodialysis:

    Hemodialysis removes significant amounts of metronidazole and its metabolites from systemic circulation. The clearance of metronidazole will depend on the type of dialysis membrane used, the duration of the dialysis session, and other factors. If the administration of metronidazole cannot be separated from the hemodialysis session, supplementation of metronidazole dosage following the hemodialysis session should be considered, depending on the patient’s clinical situation (see CLINICAL PHARMACOLOGY).

  • Upsher-smith Laboratories, Inc.
    Klor-con M | Upsher-smith Laboratories, Inc.
    No Recall

    Klor-con M | Upsher-smith Laboratories, Inc.

    Klor-con M | Upsher-smith Laboratories, Inc.

    The usual dietary intake of potassium by the average adult is 50 to 100 mEq per day. Potassium depletion sufficient to cause hypokalemia usually requires the loss of 200 or more mEq of potassium from the total body store.

    Dosage must be adjusted to the individual needs of each patient. The dose for the prevention of hypokalemia is typically in the range of 20 mEq per day. Doses of 40-100 mEq per day or more are used for the treatment of potassium depletion. Dosage should be divided if more than 20 mEq per day is given such that no more than 20 mEq is given in a single dose.

    Each Klor-Con® M20 tablet provides 1500 mg of potassium chloride equivalent to 20 mEq of potassium.

    Each Klor-Con® M15 tablet provides 1125 mg of potassium chloride equivalent to 15 mEq of potassium.

    Each Klor-Con® M10 tablet provides 750 mg of potassium chloride equivalent to 10 mEq of potassium.

    Klor-Con® M tablets should be taken with meals and with a glass of water or other liquid. This product should not be taken on an empty stomach because of its potential for gastric irritation (see WARNINGS).

    Patients having difficulty swallowing whole tablets may try one of the following alternate methods of administration:

    Break the tablet in half and take each half separately with a glass of water. Prepare an aqueous (water) suspension as follows: Place the whole tablet(s) in approximately one-half glass of water (4 fluid ounces). Allow approximately 2 minutes for the tablet(s) to disintegrate. Stir for about half a minute after the tablet(s) has disintegrated. Swirl the suspension and consume the entire contents of the glass immediately by drinking or by the use of a straw. Add another one fluid ounce of water, swirl, and consume immediately. Then, add an additional one fluid ounce of water, swirl, and consume immediately.   Aqueous suspension of Klor-Con ® M extended-release tablet that is not taken immediately should be discarded. The use of other liquids for suspending Klor-Con ® M tablets is not recommended.
  • Klor-con M | Cardinal Health
    No Recall

    Klor-con M | Cardinal Health

    Klor-con M | Cardinal Health

    The usual dietary intake of potassium by the average adult is 50 to 100 mEq per day. Potassium depletion sufficient to cause hypokalemia usually requires the loss of 200 or more mEq of potassium from the total body store.

    Dosage must be adjusted to the individual needs of each patient. The dose for the prevention of hypokalemia is typically in the range of 20 mEq per day. Doses of 40-100 mEq per day or more are used for the treatment of potassium depletion. Dosage should be divided if more than 20 mEq per day is given such that no more than 20 mEq is given in a single dose.

    Each Klor-Con® M20 tablet provides 1500 mg of potassium chloride equivalent to 20 mEq of potassium.

    Each Klor-Con® M15 tablet provides 1125 mg of potassium chloride equivalent to 15 mEq of potassium.

    Each Klor-Con® M10 tablet provides 750 mg of potassium chloride equivalent to 10 mEq of potassium.

    Klor-Con® M tablets should be taken with meals and with a glass of water or other liquid. This product should not be taken on an empty stomach because of its potential for gastric irritation (see WARNINGS).

    Patients having difficulty swallowing whole tablets may try one of the following alternate methods of administration:

    Break the tablet in half and take each half separately with a glass of water. Prepare an aqueous (water) suspension as follows: Place the whole tablet(s) in approximately one-half glass of water (4 fluid ounces). Allow approximately 2 minutes for the tablet(s) to disintegrate. Stir for about half a minute after the tablet(s) has disintegrated. Swirl the suspension and consume the entire contents of the glass immediately by drinking or by the use of a straw. Add another one fluid ounce of water, swirl and consume immediately. Then, add an additional one fluid ounce of water, swirl and consume immediately.   Aqueous suspension of Klor-Con ® M extended-release tablet that is not taken immediately should be discarded. The use of other liquids for suspending Klor-Con ® M tablets is not recommended.
  • Remedyrepack Inc.
    Klor-con M | Remedyrepack Inc.
    No Recall

    Klor-con M | Remedyrepack Inc.

    Klor-con M | Remedyrepack Inc.
    The usual dietary intake of potassium by the average adult is 50 to 100 mEq per day. Potassium depletion sufficient to cause hypokalemia usually requires the loss of 200 or more mEq of potassium from the total body store.
    Dosage must be adjusted to the individual needs of each patient. The dose for the prevention of hypokalemia is typically in the range of 20 mEq per day. Doses of 40-100 mEq per day or more are used for the treatment of potassium depletion. Dosage should be divided if more than 20 mEq per day is given such that no more than 20 mEq is given in a single dose.
    Each Klor-ConM20 tablet provides 1500 mg of potassium chloride equivalent to 20 mEq of potassium.
    Each Klor-ConM15 tablet provides 1125 mg of potassium chloride equivalent to 15 mEq of potassium.
    Each Klor-ConM10 tablet provides 750 mg of potassium chloride equivalent to 10 mEq of potassium.
    Klor-ConM tablets should be taken with meals and with a glass of water or other liquid. This product should not be taken on an empty stomach because of its potential for gastric irritation (see WARNINGS).
    Patients having difficulty swallowing whole tablets may try one of the following alternate methods of administration:
    a. Break the tablet in half and take each half separately with a glass of water.
    b. Prepare an aqueous (water) suspension as follows:
    1. Place the whole tablet(s) in approximately one-half glass of water (4 fluid ounces).
    2. Allow approximately 2 minutes for the tablet(s) to disintegrate.
    3. Stir for about half a minute after the tablet(s) has disintegrated.
    4. Swirl the suspension and consume the entire contents of the glass immediately by drinking or by the use of a straw.
    5. Add another one fluid ounce of water, swirl, and consume immediately.
    6. Then, add an additional one fluid ounce of water, swirl, and consume immediately.
    Aqueous suspension of Klor-ConM extended-release tablet that is not taken immediately should be discarded. The use of other liquids for suspending Klor-ConM tablets is not recommended.

  • Klor-con M | Unit Dose Services
    No Recall

    Klor-con M | Unit Dose Services

    Klor-con M | Unit Dose Services

    The usual dietary intake of potassium by the average adult is 50 to 100 mEq per day. Potassium depletion sufficient to cause hypokalemia usually requires the loss of 200 or more mEq of potassium from the total body store.

    Dosage must be adjusted to the individual needs of each patient. The dose for the prevention of hypokalemia is typically in the range of 20 mEq per day. Doses of 40-100 mEq per day or more are used for the treatment of potassium depletion. Dosage should be divided if more than 20 mEq per day is given such that no more than 20 mEq is given in a single dose.

    Each Potassium Chloride Extended-release Tablet, USP provides either 1500 mg of potassium chloride equivalent to 20 mEq of potassium or 750 mg of potassium chloride equivalent to 10 mEq of potassium. Potassium Chloride Extended-release Tablets, USP should be taken with meals and with a glass of water or other liquid. This product should not be taken on an empty stomach because of its potential for gastric irritation (see ). WARNINGS

    Patients having difficulty swallowing whole tablets may try one of the following alternate methods of administration:

    a. Break the tablet in half and take each half separately with a glass of water. b. Prepare an aqueous (water) suspension as follows: Place the whole tablet(s) in approximately one-half glass of water (4 fluid ounces). Allow approximately 2 minutes for the tablet(s) to disintegrate. Stir for about half a minute after the tablet(s) has disintegrated. Swirl the suspension and consume the entire contents of the glass immediately by drinking or by the use of a straw. Add another one fluid ounce of water, swirl, and consume immediately. Then, add an additional one fluid ounce of water, swirl, and consume immediately.   Aqueous suspension of Potassium Chloride Extended-release Tablets, USP that is not taken immediately should be discarded. The use of other liquids for suspending Potassium Chloride Extended-release Tablets, USP is not recommended.
  • Pd-rx Pharmaceuticals, Inc.
    Klor-con M | Pd-rx Pharmaceuticals, Inc.
    No Recall

    Klor-con M | Pd-rx Pharmaceuticals, Inc.

    Klor-con M | Pd-rx Pharmaceuticals, Inc.

    The usual dietary intake of potassium by the average adult is 50 to 100 mEq per day. Potassium depletion sufficient to cause hypokalemia usually requires the loss of 200 or more mEq of potassium from the total body store.

    Dosage must be adjusted to the individual needs of each patient. The dose for the prevention of hypokalemia is typically in the range of 20 mEq per day. Doses of 40-100 mEq per day or more are used for the treatment of potassium depletion. Dosage should be divided if more than 20 mEq per day is given such that no more than 20 mEq is given in a single dose.

    Each Klor-Con® M20 tablet provides 1500 mg of potassium chloride equivalent to 20 mEq of potassium.

    Each Klor-Con® M15 tablet provides 1125 mg of potassium chloride equivalent to 15 mEq of potassium.

    Each Klor-Con® M10 tablet provides 750 mg of potassium chloride equivalent to 10 mEq of potassium.

    Klor-Con® M tablets should be taken with meals and with a glass of water or other liquid. This product should not be taken on an empty stomach because of its potential for gastric irritation (see WARNINGS).

    Patients having difficulty swallowing whole tablets may try one of the following alternate methods of administration:

    Break the tablet in half and take each half separately with a glass of water. Prepare an aqueous (water) suspension as follows: Place the whole tablet(s) in approximately one-half glass of water (4 fluid ounces). Allow approximately 2 minutes for the tablet(s) to disintegrate. Stir for about half a minute after the tablet(s) has disintegrated. Swirl the suspension and consume the entire contents of the glass immediately by drinking or by the use of a straw. Add another one fluid ounce of water, swirl, and consume immediately. Then, add an additional one fluid ounce of water, swirl, and consume immediately.   Aqueous suspension of Klor-Con ® M extended-release tablet that is not taken immediately should be discarded. The use of other liquids for suspending Klor-Con ® M tablets is not recommended.
  • Mckesson Contract Packaging
    Klor-con M | Mckesson Contract Packaging
    No Recall

    Klor-con M | Mckesson Contract Packaging

    Klor-con M | Mckesson Contract Packaging

    The usual dietary intake of potassium by the average adult is 50 to 100 mEq per day. Potassium depletion sufficient to cause hypokalemia usually requires the loss of 200 or more mEq of potassium from the total body store.

    Dosage must be adjusted to the individual needs of each patient. The dose for the prevention of hypokalemia is typically in the range of 20 mEq per day. Doses of 40-100 mEq per day or more are used for the treatment of potassium depletion. Dosage should be divided if more than 20 mEq per day is given such that no more than 20 mEq is given in a single dose.

    Each Klor-Con® M20 tablet provides 1500 mg of potassium chloride equivalent to 20 mEq of potassium.

    Each Klor-Con® M15 tablet provides 1125 mg of potassium chloride equivalent to 15 mEq of potassium.

    Each Klor-Con® M10 tablet provides 750 mg of potassium chloride equivalent to 10 mEq of potassium.

    Klor-Con® M tablets should be taken with meals and with a glass of water or other liquid. This product should not be taken on an empty stomach because of its potential for gastric irritation (see WARNINGS).

    Patients having difficulty swallowing whole tablets may try one of the following alternate methods of administration:

    Break the tablet in half and take each half separately with a glass of water. Prepare an aqueous (water) suspension as follows: Place the whole tablet(s) in approximately one-half glass of water (4 fluid ounces). Allow approximately 2 minutes for the tablet(s) to disintegrate. Stir for about half a minute after the tablet(s) has disintegrated. Swirl the suspension and consume the entire contents of the glass immediately by drinking or by the use of a straw. Add another one fluid ounce of water, swirl, and consume immediately. Then, add an additional one fluid ounce of water, swirl, and consume immediately.   Aqueous suspension of Klor-Con ® M extended-release tablet that is not taken immediately should be discarded. The use of other liquids for suspending Klor-Con ® M tablets is not recommended.
  • Aphena Pharma Solutions – Tennessee, Inc.
    Klor-con M | Aphena Pharma Solutions - Tennessee, Inc.
    No Recall

    Klor-con M | Aphena Pharma Solutions - Tennessee, Inc.

    Klor-con M | Aphena Pharma Solutions - Tennessee, Inc.

    The usual dietary intake of potassium by the average adult is 50 to 100 mEq per day. Potassium depletion sufficient to cause hypokalemia usually requires the loss of 200 or more mEq of potassium from the total body store.

    Dosage must be adjusted to the individual needs of each patient. The dose for the prevention of hypokalemia is typically in the range of 20 mEq per day. Doses of 40-100 mEq per day or more are used for the treatment of potassium depletion. Dosage should be divided if more than 20 mEq per day is given such that no more than 20 mEq is given in a single dose.

    Each Klor-Con® M20 tablet provides 1500 mg of potassium chloride equivalent to 20 mEq of potassium.

    Each Klor-Con® M15 tablet provides 1125 mg of potassium chloride equivalent to 15 mEq of potassium.

    Each Klor-Con® M10 tablet provides 750 mg of potassium chloride equivalent to 10 mEq of potassium.

    Klor-Con® M tablets should be taken with meals and with a glass of water or other liquid. This product should not be taken on an empty stomach because of its potential for gastric irritation (see WARNINGS).

    Patients having difficulty swallowing whole tablets may try one of the following alternate methods of administration:

    Break the tablet in half and take each half separately with a glass of water. Prepare an aqueous (water) suspension as follows: Place the whole tablet(s) in approximately one-half glass of water (4 fluid ounces). Allow approximately 2 minutes for the tablet(s) to disintegrate. Stir for about half a minute after the tablet(s) has disintegrated. Swirl the suspension and consume the entire contents of the glass immediately by drinking or by the use of a straw. Add another one fluid ounce of water, swirl, and consume immediately. Then, add an additional one fluid ounce of water, swirl, and consume immediately.   Aqueous suspension of Klor-Con ® M extended-release tablet that is not taken immediately should be discarded. The use of other liquids for suspending Klor-Con ® M tablets is not recommended.
  • Aphena Pharma Solutions – Tennessee, Llc
    Klor-con M | Aphena Pharma Solutions - Tennessee, Llc
    No Recall

    Klor-con M | Aphena Pharma Solutions - Tennessee, Llc

    Klor-con M | Aphena Pharma Solutions - Tennessee, Llc

    The usual dietary intake of potassium by the average adult is 50 to 100 mEq per day. Potassium depletion sufficient to cause hypokalemia usually requires the loss of 200 or more mEq of potassium from the total body store.

    Dosage must be adjusted to the individual needs of each patient. The dose for the prevention of hypokalemia is typically in the range of 20 mEq per day. Doses of 40-100 mEq per day or more are used for the treatment of potassium depletion. Dosage should be divided if more than 20 mEq per day is given such that no more than 20 mEq is given in a single dose.

    Each Klor-Con® M20 tablet provides 1500 mg of potassium chloride equivalent to 20 mEq of potassium.

    Each Klor-Con® M15 tablet provides 1125 mg of potassium chloride equivalent to 15 mEq of potassium.

    Each Klor-Con® M10 tablet provides 750 mg of potassium chloride equivalent to 10 mEq of potassium.

    Klor-Con® M tablets should be taken with meals and with a glass of water or other liquid. This product should not be taken on an empty stomach because of its potential for gastric irritation (see WARNINGS).

    Patients having difficulty swallowing whole tablets may try one of the following alternate methods of administration:

    Break the tablet in half and take each half separately with a glass of water. Prepare an aqueous (water) suspension as follows: Place the whole tablet(s) in approximately one-half glass of water (4 fluid ounces). Allow approximately 2 minutes for the tablet(s) to disintegrate. Stir for about half a minute after the tablet(s) has disintegrated. Swirl the suspension and consume the entire contents of the glass immediately by drinking or by the use of a straw. Add another one fluid ounce of water, swirl, and consume immediately. Then, add an additional one fluid ounce of water, swirl, and consume immediately.   Aqueous suspension of Klor-Con ® M extended-release tablet that is not taken immediately should be discarded. The use of other liquids for suspending Klor-Con ® M tablets is not recommended.
  • Sandoz Inc.
    Klor-con M | Sandoz Inc.
    No Recall

    Klor-con M | Sandoz Inc.

    Klor-con M | Sandoz Inc.

    The usual dietary intake of potassium by the average adult is 50 to 100 mEq per day. Potassium depletion sufficient to cause hypokalemia usually requires the loss of 200 or more mEq of potassium from the total body store.

    Dosage must be adjusted to the individual needs of each patient. The dose for the prevention of hypokalemia is typically in the range of 20 mEq per day. Doses of 40-100 mEq per day or more are used for the treatment of potassium depletion. Dosage should be divided if more than 20 mEq per day is given such that no more than 20 mEq is given in a single dose.

    Each Klor-Con® M20 tablet provides 1500 mg of potassium chloride equivalent to 20 mEq of potassium.

    Each Klor-Con® M15 tablet provides 1125 mg of potassium chloride equivalent to 15 mEq of potassium.

    Each Klor-Con® M10 tablet provides 750 mg of potassium chloride equivalent to 10 mEq of potassium.

    Klor-Con® M tablets should be taken with meals and with a glass of water or other liquid. This product should not be taken on an empty stomach because of its potential for gastric irritation (see WARNINGS).

    Patients having difficulty swallowing whole tablets may try one of the following alternate methods of administration:

    Break the tablet in half and take each half separately with a glass of water. Prepare an aqueous (water) suspension as follows: Place the whole tablet(s) in approximately one-half glass of water (4 fluid ounces). Allow approximately 2 minutes for the tablet(s) to disintegrate. Stir for about half a minute after the tablet(s) has disintegrated. Swirl the suspension and consume the entire contents of the glass immediately by drinking or by the use of a straw. Add another one fluid ounce of water, swirl, and consume immediately. Then, add an additional one fluid ounce of water, swirl, and consume immediately.
    Aqueous suspension of Klor-Con® M extended-release tablet that is not taken immediately should be discarded. The use of other liquids for suspending Klor-Con® M tablets is not recommended.