FDA Label for Gnp Extra Strength Anti-itch Cream
View Indications, Usage & Precautions
Gnp Extra Strength Anti-itch Cream Product Label
The following document was submitted to the FDA by the labeler of this product Amerisource Bergen. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredients
Diphenhydramine hydrochloride 2%
Zinc acetate 0.1%
Ask Doctor Section
conditions worsen
symptoms last more than 7 days or clear up and occur again within a few days
Do Not Use Section
on chicken pox, poison ivy, sunburn, large areas of the body, broken, blistered, or oozing skin, more often than directed, or with any other product containing diphenhydramine, even one taken by mouth
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Warnings
For external use only
Directions
do not use more often then directed
adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily
children under 2 years: ask doctor
Uses
temporarily relieves pain and itching due to:
- insect bites
- minor burns
- sunburns
- minor skin irritations
- minor cuts
- scrapes
- rashes due to poison ivy, poison oak and poison sumac
- dries the oozing and weeping of poison:
- Ivy
- oak
- sumac
Other Safety Information
Store at 20C to 25C (68F to 77F)
Otc - Questions
www.mygnp.com
Inactive Ingredient
ceytl alcohol
diazolindinyl urea
methlparaben
polyethylene glycol
monostearate 1000
propylene glycol
propylparaben
purified water
stearyl alcohol
Otc - Purpose
Diphenhydramine hydrochloride...............Topical anagesic
Zinc acetate..............................................Skin protectant
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