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GALZIN

NDC 57844-215 · Teva Pharmaceuticals USA, Inc.

FDA lists marketing as ended on 2026-08-31.

Generic nameZinc Acetate

Dosage formCAPSULE

RouteORAL

Active ingredient(s)ZINC ACETATE

Strength25 mg/1

Pharmacologic classCopper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]

Marketing categoryNDA

Packages

57844-215-52 — 250 CAPSULE in 1 BOTTLE (57844-215-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51672-2089 — Diphenhydramine Hydrochloride and Zinc Acetate, 51824-088 — diphenhydramine hydrochloride and zinc acetate cream, 52000-071 — Itch Stopping Cream, 52651-056 — Pramoxine Hydrochloride and Zinc Acetate, 53943-258 — Diphenhydramine hydrochloride and Zinc acetate, 53943-261 — Diphenhydramine hydrochloride, Zinc acetate, 55621-007 — DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, 55910-218 — Pramoxine HCl, Zinc acetate, 55910-295 — Diphenhydramine HCl, Zinc Acetate, 57237-352 — Diphenhydramine Hydrochloride and Zinc Acetate, 59450-295 — Diphenhydramine HCl, Zinc acetate, 59555-002 — DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate, 59555-200 — ZINC ACETATE, 59640-218 — pramoxine hcl, zinc acetate lotion, 59779-708 — Diphenhydramine Hydrochloride, Zinc Acetate, 63868-952 — Diphenhydramine HCl, Zinc Acetate, 63941-259 — Diphenhydramine HCl, Zinc Acetate, 63941-549 — Extra Strength Itch Relief, 65753-400 — camphor, diphenhydramine, zinc acetate, 67091-277 — Diphenhydramine hydrochloride, and Zinc acetate, +81 more

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