Itch Relief

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Itch Relief Recall

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Side Effects & Adverse Reactions

For external use only

Do not use

on poison ivy or sunburn
on broken, blistered or oozing skin
on large areas of the body
with any other product containing diphenhydramine, even one taken by mouth

Ask a doctor before use

on chicken pox or measles

Stop use and ask a doctor if

condition worsens
symptoms persist for more than 7 days
symptoms clear up and occur again within a few days

Keep out of the reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Do not use

on poison ivy or sunburn
on broken, blistered or oozing skin
on large areas of the body
with any other product containing diphenhydramine, even one taken by mouth

Ask a doctor before use

on chicken pox or measles

Stop use and ask a doctor if

condition worsens
symptoms persist for more than 7 days
symptoms clear up and occur again within a few days

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Legal Issues

There is currently no legal information available for this drug.

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FDA Safety Alerts

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

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Manufacturer Warnings

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

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FDA Labeling Changes

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

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Uses

for temporary relief of pain and itching associated with minor burns, minor cuts, scrapes, insect bites or minor skin irritations

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History

There is currently no drug history available for this drug.

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Other Information

There are no additional details available for this product.

Sources

Itch Relief Manufacturers

Water-jel Technologies

Itch Relief | Water-jel Technologies

do not use more often than directed adults and children 2 years of age and older: apply to the affected area not more than 3 - 4 times daily children under 2 years: consult a doctor

No Recall
H E B

Itch Relief | H E B

do not use more than directed adults and children 2 years of age and older: apply to affected area no more than 3 to 4 times daily children under 2 years of age: ask a doctor

No Recall
Dolgencorp, Llc

Itch Relief | Nibec Co., Ltd

for dental use only

No Recall
American Sales Company

Itch Relief | American Sales Company

Directions
•do note use more than directed
•adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
•children under 2 years of age: ask a doctor

No Recall
Safetec Of America, Inc.

Itch Relief | Safetec Of America, Inc.

12 and over: apply to affected area not more than 3 to 4 times daily under 12: consult a doctor

No Recall
Cintas First Aid & Safety

Itch Relief | Cintas First Aid & Safety

do not use more than directed adults & children12 and over: apply to affected area not more than 3 to 4 times daily children under 12 years: consult a doctor

No Recall
Cintas First Aid & Safety

Itch Relief | Dolgencorp, Llc

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

No Recall
Cvs Pharmacy

Itch Relief | Cardinal Health

Carefully consider the potential benefits and risks of ibuprofen tablets and other treatment options before deciding to use ibuprofen tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS).

After observing the response to initial therapy with ibuprofen tablets the dose and frequency should be adjusted to suit an individual patient's needs.

Do not exceed 3200 mg total daily dose. If gastrointestinal complaints occur, administer ibuprofen tablets with meals or milk.

Rheumatoid arthritis and osteoarthritis, including flare-ups of chronic disease:

Suggested Dosage: 1200 mg-3200 mg daily (300 mg qid; 400 mg, 600 mg or 800 mg tid or qid).

Individual patients may show a better response to 3200 mg daily, as compared with 2400 mg, although in well-controlled clinical trials patients on 3200 mg did not show a better mean response in terms of efficacy.

Therefore, when treating patients with 3200 mg/day, the physician should observe sufficient increased clinical benefits to offset potential increased risk.

The dose should be tailored to each patient, and may be lowered or raised depending on the severity of symptoms either at time of initiating drug therapy or as the patient responds or fails to respond.

In general, patients with rheumatoid arthritis seem to require higher doses of ibuprofen tablets than do patients with osteoarthritis.

The smallest dose of ibuprofen tablets that yields acceptable control should be employed. A linear blood level dose-response relationship exists with single doses up to 800 mg (See CLINICAL PHARMACOLOGY for effects of food on rate of absorption).

The availability of four tablet strengths facilitates dosage adjustment.

In chronic conditions, a therapeutic response to therapy with ibuprofen tablets is sometimes seen in a few days to a week but most often is observed by two weeks. After a satisfactory response has been achieved, the patient's dose should be reviewed and adjusted as required.

Mild to moderate pain: 400 mg every 4 to 6 hours as necessary for relief of pain.

In controlled analgesic clinical trials, doses of ibuprofen tablets greater than 400 mg were no more effective than the 400 mg dose.

Dysmenorrhea: For the treatment of dysmenorrhea, beginning with the earliest onset of such pain, ibuprofen tablets should be given in a dose of 400 mg every 4 hours as necessary for the relief of pain.

No Recall