Active Ingredient
Diphenhydramine hydrochloride 2%
Zinc acetate 0.1%
The following Structured Product Label (SPL) was submitted to the FDA by Major Pharmaceuticals for the product Banophen (NDC 0904-5354). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, ask a doctor before use, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Diphenhydramine hydrochloride 2%
Zinc acetate 0.1%
Topical analgesic
Skin protectant
For external use only
If swallowed, get medical help or contact a Poison Control Center right away.
cetyl alcohol, diazolidinyl urea, methylparaben, PEG-2 stearate, PEG-20 stearate, propylene glycol, propylparaben, purified water
1-800-616-2471
Extra Strength
Banophen™
Anti-Itch Cream
Topical Analgesic/Skin Protectant
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