Laser Pharmaceuticals, Llc

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Laser Pharmaceuticals, Llc Drugs

Hemmorex-hc

Hemmorex-hc

For rectal administration. Detach one suppository from strip of suppositories. Remove the wrapper. Avoid excessive handling of the suppository which is designed to melt at body temperature. Insert suppository into the rectum with gentle pressure, pointed end first. Insert one suppository in the rectum twice daily, morning and night for two weeks, in nonspecific proctitis. In more severe cases, one suppository three times a day or two suppositories twice daily. In factitial proctitis, the recommended duration of therapy is six to eight weeks or less, according to the response of the individual case.

All prescription substitutions and/or recommendations using this product shall be made subject to state and federal statutes as applicable. Please NOTE: This is not an Orange Book product and has not been subjected to FDA therapeutic or other equivalency testing. No representation is made as to generic status or bioequivalency. Each person recommending a prescription substitution using this product shall make such recommendation based on his/her professional knowledge and opinion, upon evaluating the active ingredients, inactive ingredients, excipients and chemical information provided herein.
Hemmorex-hc

Hemmorex-hc

For rectal administration. Detach one suppository from strip of suppositories. Remove the wrapper. Avoid excessive handling of the suppository which is designed to melt at body temperature. Insert suppository into the rectum with gentle pressure, pointed end first. Insert one suppository in the rectum twice daily, morning and night for two weeks, in nonspecific proctitis. In more severe cases, one suppository three times a day or two suppositories twice daily. In factitial proctitis, the recommended duration of therapy is six to eight weeks or less, according to the response of the individual case.

All prescription substitutions and/or recommendations using this product shall be made subject to state and federal statutes as applicable. Please NOTE: This is not an Orange Book product and has not been subjected to FDA therapeutic or other equivalency testing. No representation is made as to generic status or bioequivalency. Each person recommending a prescription substitution using this product shall make such recommendation based on his/her professional knowledge and opinion, upon evaluating the active ingredients, inactive ingredients, excipients and chemical information provided herein.
Millipred

Millipred

The initial dosage of Millipred Oral Solution (10 mg Prednisolone per 5 mL) may vary from 2.5 mL to 30 mL (5 to 60 mg prednisolone base) per day depending on the specific disease entity being treated. In situations of less severity, lower doses will generally suffice while in selected patients higher initial doses may be required. The initial dosage should be maintained or adjusted until a satisfactory response is noted. If after a reasonable period of time, there is a lack of satisfactory clinical response, Millipred Oral Solution (10 mg Prednisolone per 5 mL) should be discontinued and the patient placed on other appropriate therapy. IT SHOULD BE EMPHASIZED THAT DOSAGE REQUIREMENTS ARE VARIABLE AND MUST BE INDIVIDUALIZED ON THE BASIS OF THE DISEASE UNDER TREATMENT AND THE RESPONSE OF THE PATIENT. After a favorable response is noted, the proper maintenance dosage should be determined by decreasing the initial drug dosage in small decrements at appropriate time intervals until the lowest dosage which will maintain an adequate clinical response is reached. It should be kept in mind that constant monitoring is needed in regard to drug dosage. Included in the situations which may make dosage adjustments necessary are changes in clinical status secondary to remissions or exacerbations in the disease process, the patient's individual drug responsiveness, and the effect of patient exposure to stressful situations not directly related to the disease entity under treatment; in this latter situation it may be necessary to increase the dosage of Millipred Oral Solution (10 mg Prednisolone per 5 mL) for a period of time consistent with the patient's condition. If after long term therapy the drug is to be stopped, it is recommended that it be withdrawn gradually rather than abruptly.

In the treatment of acute exacerbations of multiple sclerosis, daily doses of 200 mg of prednisolone for a week followed by 80 mg every other day or 4 to 8 mg dexamethasone every other day for one month have been shown to be effective.

In pediatric patients, the initial dose of Millipred Oral Solution (10 mg Prednisolone per 5 mL) may vary depending on the specific disease entity being treated. The range of initial doses is 0.14 to 2 mg/kg/day in three or four divided doses (4 to 60 mg/m2bsa/day).

The standard regimen used to treat nephrotic syndrome in pediatric patients is 60 mg/m2/day given in three divided doses for 4 weeks, followed by 4 weeks of single dose alternate-day therapy at 40 mg/m2/day.

The National Heart, Lung, and Blood Institute (NHLBI) recommended dosing for systemic prednisone, prednisolone or methylprednisolone in children whose asthma is uncontrolled by inhaled corticosteroids and long-acting bronchodilators is 1-2 mg/kg/day in single or divided doses. It is further recommended that short course, or "burst" therapy, be continued until a child achieves a peak expiratory flow rate of 80% of his or her personal best or symptoms resolve. This usually requires 3 to 10 days of treatment, although it can take longer. There is no evidence that tapering the dose after improvement will prevent a relapse.

For the purpose of comparison, 5 mL of Millipred Oral Solution (13.4 mg Prednisolone sodium phosphate) is equivalent to the following milligram dosage of the various glucocorticoids:
Cortisone, 50 Triamcinolone, 8 Hydrocortisone, 40 Paramethasone, 4 Prednisolone, 10 Betamethasone, 1.5 Prednisone, 10 Dexamethasone, 1.5 Methylprednisolone, 8
These dose relationships apply only to oral or intravenous administration of these compounds. When these substances or their derivatives are injected intramuscularly or into joint spaces, their relative properties may be greatly altered.
Donatuss Dc

Donatuss Dc

Adults and children over 12 years: 1 to 2 teaspoonfuls (5 mL to 10 mL) every 4 to 6 hours, as needed.

Children 6 to under 12 years of age: 1/2 to 1 teaspoonful (2.5 mL to 5 mL), every 4 to 6 hours, as needed.

Not recommended for children under 6 years of age.
Donatussin Drops

Donatussin Drops

Do not exceed recommended dosage. Use enclosed dropper only. Do not use any other dosage device. Children 6 to under 12years of age: 2 dropperfuls (2 mL) every 4 to 6 hours,not to exceed 6 doses in 24 hours. Children under 6 yearsof age: Consult a doctor.
Neo Dm Drops Dm

Neo Dm Drops Dm

Do not exceed recommended dosage. Use enclosed dropper only. Do not use any other dosage device. Children 6 to under 12 years of age: 2 dropperfuls (2 mL) every 4 to 6 hours,not to exceed 6 doses in 24 hours. Children under 6years of age: Consult a doctor
Donatussin Dm Drops Dm

Donatussin Dm Drops Dm

Do not exceed recommended dosage. Use only with enclosed dropper. Do not use with any other dosing device. Children 6 to under 12years of age: 2 dropperfuls (2 mL) every 4-6 hours, notto exceed 6 doses in 24 hours Children under 6 years of age: Consult a Doctor
Neo Ac

Neo Ac

Do not exceed recommended dosage. Adults and children 12 years of age and over: 1-2 teaspoonfuls (5-10 mL) every 4 to 6 hours, not to exceed 8 teaspoonfuls in a 24 hour period Children 6 to under 12 years of age: 1/2-1 teaspoonful (2.5-5 mL) every 4 to 6 hours, not to exceed 4 teaspoonfuls in a 24 hour period Children under 6 years of age: Consult a doctor
Donatussin

Donatussin

Do not exceed 4 doses in a 24 hour period. Adults andchildren 12 years of ageand over: 2 teaspoonfuls (10 mL)every 6 to 8 hours, not toexceed 8 teaspoonfuls in24 hours Children 6 tounder 12 yearsof age: 1 teaspoonful (5 mL)every 6 to 8 hours, not toexceed 4 teaspoonfuls in24 hours Children 2 tounder 6 yearsof age: 1/2 teaspoonful (2.5 mL)every 6 to 8 hours, not toexceed 2 teaspoonfuls in24 hours Children under2 years of age: Consult a doctor
Neo Dm

Neo Dm

Do not exceed 4 doses in a 24 hour period. Adults andchildren 12years of age and over: 1 teaspoonful (5 mL)every 6 hours, not to exceed 4 teaspoonfulsin 24 hours. Children 6to under 12years of age: 1/2 teaspoonful (2.5 mL)every 6 hours, not to exceed2 teaspoonfuls in 24 hours. Childrenunder 6years of age: Consult a physician.
Millipred

Millipred

THE INITIAL DOSAGE OF MILLIPRED AND MILLIPRED DP TABLETS MAY VARY FROM 5MG TO 60MG PER DAY DEPENDING ON THE SPECIFIC DISEASE ENTITY BEING TREATED. IN SITUATIONS OF LESS SEVERITY, LOWER DOSES WILL GENERALLY SUFFICE, WHILE IN SELECTED PATIENTS HIGHER INITIAL DOSES MAY BE REQUIRED. THE INITIAL DOSE SHOULD BE MAINTAINED OR ADJUSTED UNTIL A SATISFACTORY RESPONSE IS NOTED. IF AFTER A REASONABLE PERIOD OF TIME THERE IS A LACK OF SATISFACTORY CLINICAL RESPONSE, PREDNISOLONE SHOULD BE DISCONTINUED AND THE PATIENT TRANSFERRED TO OTHER APPROPRIATE THERAPY.IT SHOULD BE EMPHASIZED THAT DOSAGE REQUIREMENTS ARE VARIABLE AND MUST BE INDIVIDUALIZED ON THE BASIS OF THE DISEASE UNDER TREATMENT AND THE RESPONSE OF THE PATIENT.AFTER A FAVORABLE RESPONSE IS NOTED, THE PROPER MAINTENANCE DOSAGE SHOULD BE DETERMINED BY DECREASING THE INITIAL DRUG DOSE IN SMALL INCREMENTS AT APPROPRIATE TIME INTERVALS UNTIL THE LOWEST DOSAGE WHICH WILL MAINTAIN AN ADEQUATE CLINICAL RESPONSE IS REACHED. IT SHOULD BE KEPT IN MIND THAT CONSTANT MONITORING IS NEEDED IN REGARDS TO DRUG DOSAGE. INCLUDED IN THE SITUATIONS WHICH MAY MAKE DOSAGE ADJUSTMENTS NECESSARY ARE THE CHANGES IN CLINICAL STATUS SECONDARY TO REMISSIONS OR EXACERBATIONS IN THE DISEASE PROCESS, THE PATIENT'S INDIVIDUAL DRUG RESPONSIVENESS, AND THE EFFECT OF PATIENT EXPOSURE TO STRESSFUL SITUATIONS NOT DIRECTLY RELATED TO THE DISEASE ENTITY UNDER TREATMENT; IN THIS LATER SITUATION IT MAY BE NECESSARY TO INCREASE THE DOSAGE OF PREDNISOLONE FOR A PERIOD OF TIME CONSISTENT WITH THE PATIENT'S CONDITION. IF AFTER LONG-TERM THERAPY THE DRUG IS TO BE STOPPED, IT IS RECOMMENDED THAT IT BE WITHDRAWN GRADUALLY RATHER THAN ABRUPTLY.ALTERNATE-DAY THERAPYALTERNATE-DAY THERAPY IS A CORTICOSTEROID DOSING REGIMEN IN WHICH TWICE THE USUAL DAILY DOSE OF CORTICOID IS ADMINISTERED EVERY OTHER MORNING. THE PURPOSE OF THIS MODE OF THERAPY IS TO PROVIDE THE PATIENT REQUIRING LONG-TERM PHARMACOLOGIC DOSE TREATMENT WITH THE BENEFICIAL EFFECTS OF CORTICOIDS WHILE MINIMIZING CERTAIN UNDESIRABLE EFFECTS, INCLUDING PITUITARYADRENAL SUPPRESSION, THE CUSHINGOID STATE, CORTICOID WITHDRAWAL SYMPTOMS, AND GROWTH SUPPRESSION IN CHILDREN.THE RATIONALE FOR THIS TREATMENT SCHEDULE IS BASED ON TWO MAJOR PREMISES; (a) THE ANTI-INFLAMMATORY OR THERAPEUTIC EFFECT OF CORTICOIDS PERSISTS LONGER THAN THEIR PHYSICAL PRESENCE AND METABOLIC EFFECTS AND (b) ADMINISTRATION OF THE CORTICOSTEROID EVERY OTHER MORNING ALLOWS FOR RE-ESTABLISHMENT OF MORE NEARLY NORMAL HYPOTHALAMIC-PITUTARY-ADRENAL (HPA) ACTIVITY ON THE OFF-STEROID DAY.A BRIEF REVIEW OF THE HPA PHYSIOLOGY MAY BE HELPFUL IN UNDERSTANDING THIS RATIONAL. ACTING PRIMARILY THROUGH THE HYPOTHALAMUS A FALL IN FREE CORTISOL STIMULATES THE PITUITARY GLAND TO PRODUCE INCREASING AMOUNTS OF CORTICOTROPIN (ACTH) WHILE A RISE IN FREE CORTISOL INHIBITS ACTH SECRETION. NORMALLY THE HPA SYSTEM IS CHARACTERIZED BY DIURNAL (CIRCADIAN) RHYTHM. SERUM LEVELS OF ACTH RISE FROM A LOW POINT ABOUT 10 p.m. TO A PEAK LEVEL ABOUT 6 a.m. INCREASING LEVELS OF ACTH STIMULATE ADRENOCORTICAL ACTIVITY RESULTING IN A RISE IN PLASMA CORTISOL WITH A MAXIMAL LEVELS OCCURING BETWEEN 2 a.m. AND 8 a.m. THIS RISE IN CORTISOL DAMPENS ACTH PRODUCTION AND IN TURN ADRENOCORTICAL ACTIVITY. THERE IA A GRADUAL FALL IN PLASMA CORTICOIDS DURING THE DAY, THE LOWEST LEVELS OCCURRING ABOUT MIDNIGHT. THE DIURNAL RHYTHM OF THE HPA AXIS IN CUSHING'S DISEASE, A SYNDROME OF ADRENOCORTICAL HYPERFUNCTION CHARACTERIZED BY OBESITY WITH CENTRIPETAL FAT DISTRIBUTION, THINNING OF THE SKIN WITH EASY BRUISABILITY, MUSCLE WASTING AND WEAKNESS, HYPERTENSION, LATENT DIABETES, OSTEOPOROSIS, ELECTROLYTE IMBALANCES, ETC. THE SAME CLINICAL FINDINGS OF HYPERADRENOCORTICISM MAY BE NOTED DURING THE LONG-TERM PHARMACOLOGIC DOSE CORTICOID THERAPY ADMINISTERED IN CONVENTIONAL DAILY DIVIDED DOSES. IT WOULD APPEAR THEN, THAT A DISTURBANCE IN THE DIURNAL CYCLE WITH MAINTENANCE OF ELEVATED CORTICOID VALUES DURING THE NIGHT MAY PLAY A SIGNIFICANT ROLE IN THE DEVELOPMENT OF UNDESIRABLE CORTICOID EFFECTS. ESCAPE FROM THESE CONSTANTLY ELEVATED PLASMA LEVELS FOR EVEN SHORT PERIODS OF TIME MAY BE INSTRUMENTAL IN PROTECTING AGAINST UNDESIRABLE PHARMACOLOGIC EFFECTS.DURING CONVENTIONAL PHARMACOLOGIC DOSE CORTICOSTEROID THERAPY, ACTH PRODUCTION IS INHIBITED WITH SUBSEQUENT SUPPRESSION OF CORTISOL PRODUCTION BY THE ADRENAL CORTEX. RECOVERY TIME FOR NORMAL HPA ACTIVITY IS VARIABLE DEPENDING UPON THE DOSE AND DURATION OF TREATMENT.DURING THIS TIME THE PATIENT IS VULENERABLE TO ANY STRESSFUL SITUATION.ALTHOUGH IT HAS BEEN SHOWN THAT THERE IS CONSIDERABLY LESS ADRENAL SUPPRESSION FOLLOWING A SINGLE MORNING DOSE OF PREDNISOLONE (10 MG) AS OPPOSED TO A QUARTER OF THAT DOSE ADMINISTERED EVERY 6 HOURS, THERE IS EVIDENCE THAT SOME SUPPRESSIVE EFFECT ON ADRENAL ACTIVITY MAY BE CARRIED OVER INTO THE FOLLOWING DAY WHEN PHARMACOLOGIC DOSES ARE USED. FURTHER, IT HAS BEEN SHOWN THAT A SINGLE DOSE OF A CERTAIN CORTICOSTEROIDS WILL PRODUCE ADRENOCORTICAL SUPPRESSION FOR TWO OR MORE DAYS. OTHER CORTICOIDS, INCLUDING METHYLPREDNISOLONE, HYDROCORTISONE, PREDNISONE, AND PREDNISOLONE, ARE CONSIDERED TO BE SHORT ACTING (PRODUCING ADRENOCORTICAL SUPPRESSION FOR 1 1/4 DAYS TO 1 1/2 DAYS FOLLOWING A SINGLE DOSE) AND THUS ARE RECOMMENDED FOR ALTERNATE-DAY THERAPY.THE FOLLOWING SHOULD BE KEPT IN MIND WHEN CONSIDERING ALTERNATE-DAY THERAPY:1. BASIC PRINCIPLES AND INDICATIONS FOR CORTICOSTEROID THERAPY SHOULD APPLY. THE BENEFITS OF ALTERNATE-DAY THERAPY SHOULD NOT ENCOURAGE THE INDISCRIMINATE USE OF STEROIDS.2. ALTERNATE-DAY THERAPY IS A THERAPEUTIC TECHNIQUE PRIMARILY DESIGNED FOR PATIENTS IN WHOM LONG-TERM PHARMACOLOGIC CORTICOID THERAPY IS ANTICIPATED.3. IN LESS SEVERE DISEASE PROCESSES IN WHICH CORTICOID THERAPY IS INDICATED, IT MAY BE POSSIBLE TO INITIATE TREATMENT WITH ALTERNATE-DAY THERAPY. MORE SEVERE DISEASE STATES USUALLY WILL REQUIRE DAILY DIVIDED HIGH DOSE THERAPY FOR INITIAL CONTROL OF THE DISEASE PROCESS. THE INITIAL SUPPRESSIVE DOSE LEVEL SHOULD BE CONTINUED UNTIL SATISFACTORY CLINICAL RESPONSE IS OBTAINED, USUALLY FOUR TO TEN DAYS IN THE CASE OF MANY ALLERGIC AND COLLAGEN DISEASES. IT IS IMPORTANT TO KEEP THE PERIOD OF INITIAL SUPPRESSIVE DOSE AS BRIEF AS POSSIBLE PARTICULARLY WHEN SUBSEQUENT USE OF ALTERNATE-DAY THERAPY IS INTENDED.ONCE CONTROL HAS BEEN ESTABLISHED, TWO COURSES ARE AVAILABLE: (a) CHANGE TO ALTERNATE-DAY THERAPY AND THEN GRADUALLY REDUCE THE AMOUNT OF CORTICOID GIVEN EVERY OTHER DAY, OR (b) FOLLOWING THE COURSE OF THE DISEASE PROCESS, REDUCE THE DAILY DOSE OF CORTICOID TO THE LOWEST EFFECTIVE LEVEL AS RAPIDLY AS POSSIBLE AND THEN CHANGE OVER TO ALTERNATE-DAY SCHEDULE. THEORETICALLY, COURSE (a) MAY BE PREFERABLE. 4. BECAUSE OF THE ADVANTAGES OF ALTERNATE-DAY THERAPY, IT MAY BE DESIRABLE TO TRY PATIENTS ON THIS FORM OF THERAPY WHO HAVE BEEN ON DAILY CORTICOIDS FOR LONG PERIODS OF TIME (E.G. PATIENTS WITH RHEUMATOID ARTHRITIS). SINCE THESE PATIENTS MAY ALREADY HAVE A SUPPRESSED PA AXIS, ESTABLISHING THEM ON ALTERNATE-DAY THERAPY MAY BE DIFFICULT AND NOT ALWAYS SUCCESSFUL. HOWEVER, IT IS RECOMMENDED THAT REGULAR ATTEMPTS BE MADE TO CHANGE THEM OVER. IT MAY BE HELPFUL TO TRIPLE OR EVEN QUADRUPLE THE DAILY MAINTENANCE DOSE AND ADMINISTER THIS EVERY OTHER DAY RATHER THAN JUST DOUBLING THE DAILY DOSE IF DIFFICULTY IS ENCOUNTERED. ONCE THE PATIENT IS AGAIN CONTROLLED, AN ATTEMPT SHOULD BE MADE TO REDUCE THIS DOSE TO A MINIMUM.5. AS INDICATED ABOVE, CERTAIN CORTICOIDS, BECAUSE OF THEIR PROLONGED SUPPRESSIVE EFFECT ON ADRENAL ACTIVITY, ARE NOT RECOMMENDED FOR ALTERNATE-DAY THERAPY (E.G., DEXMETHOSONE AND BETAMETHASONE).6. THE MAXIMAL ACTIVITY OF THE ADRENAL CORTEX IS BETWEEN 2 a.m. AND 8 a.m., AND IT IS MINIMAL BETWEEN 4 p.m. AND MIDNIGHT. EXOGENOUS CORTICOSTEROIDS SUPPRESS ADRENALCORTICAL ACTIVITY THE LEAST, WHEN GIVEN AT THE TIME OF MAXIMAL ACTIVITY (a.m.).7. IN USING ALTERNATE-DAY THERAPY IT IS IMPORTANT, AS IN ALL THERAPEUTIC SITUATIONS, IN INDIVIDUALIZE AND TAILOR THE THERAPY TO EACH PATIENT. COMPLETE CONTROL OF SYMPTOMS WILL NOT BE POSSIBLE IN ALL PATIENTS. AN EXPLANATION OF THE BENEFITS OF ALTERNATE-DAY THERAPY WILL HELP THE PATIENT TO UNDERSTAND AND TOLERATE THE POSSIBLE FLARE-UP IN SYMPTOMS WHICH MAY OCCUR IN THE LATER PART OF THE OFF-STEROID DAY.OTHER SYMPTOMATIC THERAPY MAY BE ADDED OR INCREASED AT THIS TIME IF NEEDED.8. IN THE EVENT OF AN ACUTE FLARE-UP OF THE DISEASE PROCESS, IT MAY BE NECESSARY TO RETURN TO A FULL SUPPRESSIVE DAILY DIVIDED CORTICOID DOSE FOR CONTROL. ONCE CONTROL IS AGAIN ESTABLISHED, ALTERNATE-DAY THERAPY MAY BE REINSTITUTED.9. ALTHOUGH MANY OF THE UNDESIRABLE FEATURES OF CORTICOSTEROID THERAPY CAN BE MINIMIZED BY ALTERNATE-DAY THERAPY, AS IN ANY THERAPEUTIC SITUATION, THE PHYSICIAN MUST CAREFULLY WEIGH THE BENEFIT-RISK RATIO FOR EACH PATIENT WITH WHOM CORTICOID THERAPY IS BEING CONSIDERED.
Cyclivert

Cyclivert

Directions

Adults and children 12 years of age and over: 2 tablets every 4-6 hours, not to exceed 8 tablets in 24 hours.

Children 6 to under 12 years of age: 1 tablet every 6-8 hours, not to exceed 3 tablets in 24 hours.

Children under 6 years of age: Consult a physician.
Dallergy

Dallergy

Directions

Do not exceed 3 doses in a 24 hour period.

Adults and children 12 years of age and over: 2 tablets every 6-8 hours, not to exceed 6 tablets in 24 hours.

Children 6 to under 12 years of age: 1 tablet every 6-8 hours, not to exceed 3 tablets in 24 hours.

Children 2 to under 6 years of age: 1/2 tablet every 6-8 hours, not to exceed 1-1/2 tablets in 24 hours.

Children under 2 years of age: Consult a doctor.
Respaire-30

Respaire-30

Directions

take with a full glass of water this product can be administered without regard for timing of meals

adults and children 12 years of age and older 1 or 2 capsules every 4-6 hours: not more than 8 capsules in 24 hours

children 6 to under 12 years of age 1 capsule every 4-6 hours: not more than 4 capsules in 24 hours

children under 6 years of age do not use
Care One Ibuprofen Infa...

Care One Ibuprofen Infants

The usual dietary potassium intake 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.

K-Sol™ 10% To minimize gastrointestinal irritation, patients must follow directions regarding dilution. Each tablespoonful (15 mL) should be diluted with three (3) fluid ounces or more of water or other liquid.

One (1) tablespoonful (15 mL) twice daily (after morning and evening meals) supplies 40 mEq of potassium chloride.

K-Sol™ 20% To minimize gastrointestinal irritation, patients must follow directions regarding dilution. Each tablespoonful should be diluted with six (6) fluid ounces or more of water or other liquid.

One (1) tablespoonful (15 mL) per day (after the morning meal) supplies 40 mEq of potassium chloride. One tablespoonful twice a day, provides 80 mEq of potassium chloride.

Deviations from these recommendations may be indicated, since no average total daily dose can be defined but must be governed by close observation for clinical effects. However, potassium intoxication may result from any therapeutic dosage. See OVERDOSAGE and PRECAUTIONS.
Dallergy

Dallergy

Do not exceed 3 doses in a 24 hour period. Adults andchildren 12years of ageand over: 2 teaspoonfuls (10 mL)every 6 to 8 hours, not toexceed 6 teaspoonfuls in24 hours Children under 12 years of age: Consult a doctor
Dallergy Drops

Dallergy Drops

Do not exceed recommended dosage. Dosages may be repeated every 4-6 hours if required for relief. Use enclosed dropper only. Do not use any other dosage device. Adults and Children12 years of age and over: 4 dropperfuls (4 mL) every 4 hours.Not to exceed more than 6 doses in24 hours. Children 6 to under12 years of age: 2 dropperfuls (2 mL) every 4 hours.Not to exceed more than 6 doses in24 hours. Children under6 years of age: Consult a doctor
Dallergy

Dallergy

Adults and children12 years of ageand over: 2 tabletevery 4 hours,not to exceed12 tabletsin 24 hours. Children 6 to under12 years of age: 1 tabletevery 4 hours,not to exceed6 tablets in24 hours. Children under6 years of age: Consult adoctor.
Do not exceed 6 doses in a 24 hour period.
Donatussin

Donatussin

Adults and children

12 years of age

and over:

1 teaspoonful (5 mL)

every 4 hours, not to

exceed 6 teaspoonfuls

in 24 hours

Children 6 to

under 12 years

of age:

1/2 teaspoonful (2.5 mL)

every 4 hours, not to

exceed 3 teaspoonfuls

in 24 hours

Children under

6 years of age:
Consult a doctor
Dallergy

Dallergy

Directions

Laser Pharmaceuticals, Llc

Manufacturer Details

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Laser Pharmaceuticals, Llc Drugs