Anti-Itch description, usages, side effects, indications, overdosage, supplying and lots more!

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Anti-Itch

Preferred Plus (Kinray)

Anti-Itch Cream Extra Strength




FULL PRESCRIBING INFORMATION

Drug Facts

Diphenhydramine hydrochloride, USP 2%
Zinc acetate, USP 0.1%

Topical analgesic
Skin protectant

For the temporary relief of pain and itching associated with
•minor burns
•sunburn
•minor cuts
•scrapes
•insect bites
•minor skin irritations
•rashes due to poison ivy, oak and sumac
•dries the oozing and weeping of poison:
    •ivy
    •oak
    •sumac

For external use only

•on large areas of the body
•with any other product containing diphenhydramine, even one taken by mouth

•on chicken pox
•on measles

•avoid contact with the eyes

•condition gets worse
•symptoms persist for more than 7 days or clear up and occur again within a few days

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

•do not use more often 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

•Store between 59°-86°F (15°-30°C).

cetyl alcohol, methylparaben, polysorbate 60, propylene glycol, purified water, sorbitan monostearate

1-800-432-8534 between 9 am and 4 pm EST, Monday – Friday.

Preferred Plus Pharmacy®

NDC 61715-082-01
Compare to the active ingredients
 in Benadryl® Extra Strength
Itch Stopping Cream*

Extra Strength
Anti- Itch Cream

Diphenhydramine Hydrochloride, USP 2%/ Zinc Acetate, USP 0.1%

Temporary Relief of Itch and Pain due to:

• Insect Bites  • Minor Skin Irritations
• Rashes from Poison Ivy, Poison Oak or Poison Sumac

Topical Analgesic /Skin Protectant 

NET WT 1 OZ (28g)

Anti-Itch

Anti-Itch

Diphenhydramine Hydrochloride and Zinc Acetate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:61715-082
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 2 mg
ZINC ACETATE zinc 1 mg

Inactive Ingredients

Ingredient Name Strength
CETYL ALCOHOL
METHYLPARABEN
POLYSORBATE 60
propylene glycol
water
SORBITAN MONOSTEARATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 28 in 1 TUBE
2 NDC:61715-082-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2014-06-01


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Be sure to consult your doctor before taking any medication!
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