Diphenhydramine Hydrochloride and Zinc Acetate
NDC 51672-2089 · Sun Pharmaceutical Industries, Inc.
Packages
51672-2089-2 — 1 TUBE in 1 CARTON (51672-2089-2) / 28.4 g in 1 TUBE
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
51316-779 — Diphenhydramine Hydrochloride, 51316-799 — Diphenhydramine HCl, 51316-835 — Diphenhydramine Hydrochloride, 51316-863 — Acetaminophen, Diphenhydramine HCL, 51316-998 — Diphenhydramine Hydrochloride, 51662-1219 — DIPHENHYDRAMINE HYDROCHLORIDE, 51662-1348 — DIPHENHYDRAMINE HYDROCHLORIDE, 51662-1374 — DIPHENHYDRAMINE HYDROCHLORIDE, 51662-1628 — Diphenhydramine HYDROCHLORIDE, 51662-1674 — diphenhydramine hydrochloride, 51824-056 — Diphenhydramine Hydrochloride, 51824-069 — Acetaminophen, Diphenhydramine HCl, 51824-088 — diphenhydramine hydrochloride and zinc acetate cream, 51824-102 — Diphenhydramine Hydrochloride, 51824-107 — Acetaminophen, Diphenhydramine HCl, 51824-108 — Acetaminophen, Diphenhydramine HCl, 51879-802 — Diphenhydramine Hydrochloride, 52000-071 — Itch Stopping Cream, 52651-056 — Pramoxine Hydrochloride and Zinc Acetate, 53041-633 — Diphenhydramine HCl, +1060 more