Home NDC 51672-2089 Diphenhydramine Hydrochloride and Zinc Acetate
Product NDC 51672-2089
11-digit product format 516722089
Labeler code 51672
Product ID 51672-2089_38e51539-2525-fa76-e063-6294a90a6b0a
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine Hydrochloride and Zinc Acetate
Dosage form CREAM
Route TOPICAL
Labeler Sun Pharmaceutical Industries, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-09-20
Substance DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Active strength 20; 1 mg/g; mg/g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Diphenhydramine Hydrochloride and Zinc Acetate
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 20 mg/g ZINC ACETATE 1 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination TC2D6JAD40 Internal UNII lookup FM5526K07A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1087026 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51672-2089-2 Diphenhydramine Hydrochloride and Zinc Acetate 1 in 1 CARTON CREAM 1 6 51672-2089-2 Diphenhydramine Hydrochloride and Zinc Acetate 28.4 g in 1 TUBE CREAM 28.4 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Diphenhydramine Hydrochloride ACTIVE INGREDIENT TC2D6JAD40 DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 3 Zinc Acetate ACTIVE INGREDIENT FM5526K07A DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 3 Diphenhydramine ACTIVE MOIETY 8GTS82S83M DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 3 zinc cation ACTIVE MOIETY 13S1S8SF37 DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 3 cetyl alcohol INACTIVE INGREDIENT 936JST6JCN DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 3 glyceryl monostearate INACTIVE INGREDIENT 230OU9XXE4 DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 3 methylparaben INACTIVE INGREDIENT A2I8C7HI9T DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 3 PEG-100 stearate INACTIVE INGREDIENT YD01N1999R DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 3 propylene glycol INACTIVE INGREDIENT 6DC9Q167V3 DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 3 propylparaben INACTIVE INGREDIENT Z8IX2SC1OH DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 3 water INACTIVE INGREDIENT 059QF0KO0R DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51672-2089 DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 5 Current NDC, Legacy NDC, 2 package rows 20241105_c89e3de8-7d71-485c-8fc5-2832d6024f16.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 111 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Medicated Pain Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE Meijer Distribution Inc 75c6fcd5-185c-4203-b604-19ce801c865f 2024-12-18 Warnings Exact identifier application number: M017 MEIJER PAIN RELIEF PATCHES LIDOCAINE Meijer Distribution Inc aa5da66d-3ba9-4120-be35-44bec475761a 2024-12-18 Warnings Exact identifier application number: M017 Lidocaine Pain Relief Roll-On LIDOCAINE 4% CVS Pharmacy 8a9757e3-0bfc-a1e2-e053-2a95a90a6da3 2024-12-18 Warnings Exact identifier application number: M017 Dollar General Cold-Hot Medicated Patches MENTHOL DOLGENCORP, LLC c6e0388b-af9e-4e51-8f94-6788185c31a0 2024-12-18 Warnings Exact identifier application number: M017 THERA CARE PAIN THERAPY LIDOCAINE Veridian Healthcare e023bb5a-a4bc-4681-a1f4-48ca0d2cb102 2024-12-18 Warnings Exact identifier application number: M017 TheraCare Medicated Pain Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE Veridian Healthcare f6f3c9c0-d6e3-75a3-e053-6294a90a1965 2024-12-18 Warnings Exact identifier application number: M017 Good Sense Hot and Cold Medicated Patch MENTHOL GOOD SENSE 1b16c3e5-a29f-4043-94e6-0a0e0ea3d93e 2024-12-18 Warnings Exact identifier application number: M017 Hunter Beach 4% LIDOCAINE HUNTERS BEACH LIFE f2ef9c12-6e42-486b-b6f2-0ad534e94294 2024-12-18 Warnings Exact identifier application number: M017 Hunter Beach 4% LIDOCAINE HUNTERS BEACH LIFE 05a9605b-0d01-4333-8e54-7202e7c31c49 2024-12-18 Warnings Exact identifier application number: M017 Ultra Strength Muscle Rub CAMPHOR, MENTHOL, METHYL SALICYLATE The Mentholatum Company 32b64985-0e2f-49ee-9840-946d7279fee7 2024-12-17 Warnings Exact identifier application number: M017 WellPatch Warming Pain Relief CAPSAICIN The Mentholatum Company ec583129-55fc-4ab1-94e5-9c900b5d95ef 2024-12-17 Warnings Exact identifier application number: M017 CVS Health Cold and Hot Pain Relieving Extra Strength MENTHOL, METHYL SALICYLATE CVS Pharmacy 1ca1a631-cb2c-46cd-bd41-05469b08d208 2024-12-17 Warnings Exact identifier application number: M017 Mentholatum Pain Relieving MENTHOL, METHYL SALICYLATE The Mentholatum Company 0056b952-9870-485a-9f35-f985472875a9 2024-12-17 Warnings Exact identifier application number: M017 Mentholatum Lidocaine Heat LIDOCAINE HCL The Mentholatum Company cc2ef25a-b569-4d48-a666-899f710b4b34 2024-12-17 Warnings Exact identifier application number: M017 Rite Aid Muscle Rub Ultra Strength CAMPHOR, MENTHOL, METHYL SALICYLATE Rite Aid Corporation 039fff40-b5ba-42cb-932c-8a70ca92759d 2024-12-17 Warnings Exact identifier application number: M017 Signature Care Cold and Hot Medicated MENTHOL Safeway 88f59f95-0a7c-458c-949c-0dff16ad94e4 2024-12-17 Warnings Exact identifier application number: M017 Equate Cool and Heat MENTHOL, METHYL SALICYLATE Wal-Mart Stores Inc c5ab2426-eeca-4ba4-9f00-7790d2176471 2024-12-17 Warnings Exact identifier application number: M017 Equate Capsaicin Pain Relieving CAPSAICIN Wal-Mart Stores Inc 745b2cf5-2599-4383-818b-19fed248a11f 2024-12-17 Warnings Exact identifier application number: M017 CVS Health Muscle Rub Ultra Strength CAMPHOR, MENTHOL, METHYL SALICYLATE CVS Pharmacy 4fc0d6bb-efa7-40cf-a6d5-e0feaa93c80a 2024-12-17 Warnings Exact identifier application number: M017 DG Health Maximum Strength Pain Relieving Cleansing BENZALKONIUM CL, LIDOCAINE HCL Dollar General Corporation 64f69315-77a3-49dc-940d-efd7a29c6645 2024-12-17 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 51672-2089-2 51672208902 1 TUBE in 1 CARTON (51672-2089-2) / 28.4 g in 1 TUBE 1 tube 2005-09-20 0000-00-00 No No Current