diphenhydramine hydrochloride and zinc acetate

Generic: diphenhydramine hydrochloride and zinc acetate

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name diphenhydramine hydrochloride and zinc acetate
Generic Name diphenhydramine hydrochloride and zinc acetate
Labeler sun pharmaceutical industries, inc.
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

diphenhydramine hydrochloride 20 mg/g, zinc acetate 1 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-2089
Product ID 51672-2089_38e51539-2525-fa76-e063-6294a90a6b0a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2005-09-20

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516722089
Hyphenated Format 51672-2089

Supplemental Identifiers

RxCUI
1087026
UNII
TC2D6JAD40 FM5526K07A

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name diphenhydramine hydrochloride and zinc acetate (source: ndc)
Generic Name diphenhydramine hydrochloride and zinc acetate (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/g
  • 1 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51672-2089-2) / 28.4 g in 1 TUBE
source: ndc

Packages (1)

51672-2089-2 1 TUBE in 1 CARTON (51672-2089-2) / 28.4 g in 1 TUBE

Ingredients (2)

diphenhydramine hydrochloride (20 mg/g) zinc acetate (1 mg/g)

Linked Drug Pages (1)

Diphenhydramine Hydrochloride and Zinc Acetate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "38e51539-2525-fa76-e063-6294a90a6b0a", "openfda": {"unii": ["TC2D6JAD40", "FM5526K07A"], "rxcui": ["1087026"], "spl_set_id": ["c89e3de8-7d71-485c-8fc5-2832d6024f16"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-2089-2)  / 28.4 g in 1 TUBE", "package_ndc": "51672-2089-2", "marketing_start_date": "20050920"}], "brand_name": "Diphenhydramine Hydrochloride and Zinc Acetate", "product_id": "51672-2089_38e51539-2525-fa76-e063-6294a90a6b0a", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51672-2089", "generic_name": "Diphenhydramine Hydrochloride and Zinc Acetate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diphenhydramine Hydrochloride and Zinc Acetate", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/g"}, {"name": "ZINC ACETATE", "strength": "1 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20050920", "listing_expiration_date": "20261231"}