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Itch Relief

NDC 41250-295 · Meijer, Inc.

Generic nameDiphenhydramine HCl, Zinc Acetate
Dosage formSPRAY
RouteTOPICAL
Active ingredient(s)DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE
Strength20; 1 mg/mL; mg/mL
Pharmacologic classCopper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

41250-295-20 — 59 mL in 1 BOTTLE, SPRAY (41250-295-20)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41226-613 — Diphenhyramine Hydrochloride, 41226-669 — Diphenhydramine Hydrochloride, 41226-710 — Diphenhydramine hydrochloride, 41226-730 — DIPHENHYDRAMINE HYDROCHLORIDE, 41226-888 — Diphenhydramine Hydrochloride, Zinc acetate, 41250-044 — Diphenhydramine HCl, 41250-058 — Extra Strength Itch Relief, 41250-195 — Acetaminophen and Diphenhydramine Hydrochloride, 41250-218 — Pramoxine HCl, Zinc acetate, 41250-285 — IBUPROFEN, DIPHENHYDRAMINE HCL, 41250-379 — Diphenhydramine Hydrochloride, 41250-479 — Diphenhydramine Hydrochloride, 41250-526 — diphenhydramine hydrochloride, naproxen sodium, 41250-614 — diphenhydramine HCl, 41250-622 — Diphenhydramine Hydrochloride, Zinc Acetate, 41250-710 — Diphenhydramine HCl, 41250-738 — Diphenhydramine hydrochloride, 41250-853 — DIPHENHYDRAMINE HYDROCHLORIDE, 41520-034 — Diphenhydramine HCl, 41520-264 — diphenhydramine hydrochloride, naproxen sodium, +1060 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.