Active Ingredient
Diphenhydramine hydrochloride, USP 2%
Zinc acetate, USP 0.1%
The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Company for the product Wal-dryl (NDC 0363-0122). 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, USP 2%
Zinc acetate, USP 0.1%
Topical analgesic
Skin protectant
For the temporary relief of pain and itching associated with
For external use only
If swallowed, get medical help or contact a Poison Control Center right away.
cetyl alcohol, methylparaben, polysorbate 60, propylene glycol, purified water, sorbitan monostearate
NDC 0363-0525-56
Walgreens The Brand America Trusts®
Compare to the active ingredients inBENADRYL® EXTRA STRENGTH ITCH STOPPING CREAM*
Wal-dryl
Topical Analgesic/Skin Protectant
ITCH RELIEF
MAXIMUM STRENGTH
2% Diphenhydramine Hydrochloride, USP and 0.1% Zinc Acetate, USP
Temporary Relief of Itch and Pain due to
• Insect Bites • Minor Skin Irritations •Rashes from Poison Ivy, Poison Oak or Poison Sumac
PHARMACIST RECOMMENDED
NET WT. 1 OZ (28 g)
05250111F1 VC110348
*This product is not affiliated with, manufactured by, or produced by the makers or owners of Benadryl®.
Made in USA
Distributed by: Walgreen Co.,
200 Wilmot Rd., Deerfield, IL 60015-4616
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