FDA Label for Anti Itch
View Indications, Usage & Precautions
Anti Itch Product Label
The following document was submitted to the FDA by the labeler of this product Kareway Product, Inc.. 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 (In Each Gram)
Diphenhydramine HCl 2%
Zinc acetate 0.1%
Purposes
Topical analgesic
Skin protectant
Uses
- temporarily relieves itching and pain associated with insect bites, minor skin irritations and rashes due to poison ivy, poison oak or poison sumac
- dries the oozing and weeping of poison ivy, poison oak, and poison sumac
Warnings
For external use only
Do Not Use
- on chicken pox or measles
- with any other product containing diphenhydramine, even one taken by mouth
- on large areas of the body, including large areas of poison ivy, sunburn, or broken, blistered or oozing skin
Stop Use And Ask A Doctor If
- condition worsens or does not improve within 7 days
- symptoms persist for more than 7 days or clear up and occur again within a few days
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
- adults and children 12 years of age and over: apply to affected area not more than 3 to 4 times daily
- children under 12 years of age: ask a doctor
- do not use more often than directed
Other Information
- store at 59° to 77°F
Inactive Ingredients
Carbomer 940, Cetyl alcohol, Glycerin, Glyceryl monostearate, Light liquid paraffin, Methylparaben, Myristoyl/palmitoyl oxostearamide/ arachamide MEA, PEG-15 glyceryl stearate, Stearic acid, Propylparaben, Purified water
Package Label
Anti-Itch Cream
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