benadryl original strength itch stopping

Generic: diphenhydramine hydrochloride and zinc acetate

Labeler: kenvue brands llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name benadryl original strength itch stopping
Generic Name diphenhydramine hydrochloride and zinc acetate
Labeler kenvue brands llc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

diphenhydramine hydrochloride 10 mg/g, zinc acetate 1 mg/g

Manufacturer
Kenvue Brands LLC

Identifiers & Regulatory

Product NDC 69968-0625
Product ID 69968-0625_27cdd95f-6e4d-7241-e063-6394a90a5f12
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2020-01-31

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 699680625
Hyphenated Format 69968-0625

Supplemental Identifiers

RxCUI
1292313 1293717
UPC
0312547171625
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 benadryl original strength itch stopping (source: ndc)
Generic Name diphenhydramine hydrochloride and zinc acetate (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/g
  • 1 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (69968-0625-1) / 28.3 g in 1 TUBE
source: ndc

Packages (1)

69968-0625-1 1 TUBE in 1 CARTON (69968-0625-1) / 28.3 g in 1 TUBE

Ingredients (2)

diphenhydramine hydrochloride (10 mg/g) zinc acetate (1 mg/g)

Linked Drug Pages (1)

Benadryl Original Strength Itch Stopping ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "27cdd95f-6e4d-7241-e063-6394a90a5f12", "openfda": {"upc": ["0312547171625"], "unii": ["TC2D6JAD40", "FM5526K07A"], "rxcui": ["1292313", "1293717"], "spl_set_id": ["920c50cb-9bdd-4a36-bb3d-c2559db73327"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69968-0625-1)  / 28.3 g in 1 TUBE", "package_ndc": "69968-0625-1", "marketing_start_date": "20200131"}], "brand_name": "Benadryl Original Strength Itch Stopping", "product_id": "69968-0625_27cdd95f-6e4d-7241-e063-6394a90a5f12", "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": "69968-0625", "generic_name": "Diphenhydramine Hydrochloride and Zinc Acetate", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Original Strength Itch Stopping", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "10 mg/g"}, {"name": "ZINC ACETATE", "strength": "1 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200131", "listing_expiration_date": "20261231"}