Other
Drug Facts
Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558
The following Structured Product Label (SPL) was submitted to the FDA by Kenvue Brands Llc for the product Benadryl Original Strength Itch Stopping (NDC 69968-0625). 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 other, otc - purpose, uses, warnings, do not use, ask a doctor before use, otc - when using, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558
| Active ingredients | Purpose |
|---|---|
| Diphenhydramine hydrochloride 1% | Topical analgesic |
| Zinc acetate 0.1% | Skin protectant |
For external use only.
When using this product avoid contact with eyes
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
cetyl alcohol, diazolidinyl urea, methylparaben, polyethylene glycol monostearate 1000, propylene glycol, propylparaben, purified water
call toll-free 800-524-2624 (English/Spanish) or 877-717-2824 (collect)
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