benadryl extra strength itch relief

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 extra strength itch relief
Generic Name diphenhydramine hydrochloride and zinc acetate
Labeler kenvue brands llc
Dosage Form SOLUTION
Routes
TOPICAL
Active Ingredients

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

Manufacturer
Kenvue Brands LLC

Identifiers & Regulatory

Product NDC 69968-0459
Product ID 69968-0459_399004db-8df3-c030-e063-6294a90a260b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2019-06-01

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 699680459
Hyphenated Format 69968-0459

Supplemental Identifiers

RxCUI
1294589 1294591
UPC
0312547171403
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 extra strength itch relief (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/mL
  • 1 mg/mL
source: ndc
Packaging
  • 1 APPLICATOR in 1 CARTON (69968-0459-1) / 14 mL in 1 APPLICATOR
source: ndc

Packages (1)

69968-0459-1 1 APPLICATOR in 1 CARTON (69968-0459-1) / 14 mL in 1 APPLICATOR

Ingredients (2)

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

Linked Drug Pages (1)

Benadryl Extra Strength Itch Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "399004db-8df3-c030-e063-6294a90a260b", "openfda": {"upc": ["0312547171403"], "unii": ["TC2D6JAD40", "FM5526K07A"], "rxcui": ["1294589", "1294591"], "spl_set_id": ["309d9be0-e367-429a-a1fa-ab7855477c8a"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 APPLICATOR in 1 CARTON (69968-0459-1)  / 14 mL in 1 APPLICATOR", "package_ndc": "69968-0459-1", "marketing_start_date": "20190601"}], "brand_name": "Benadryl Extra Strength Itch Relief", "product_id": "69968-0459_399004db-8df3-c030-e063-6294a90a260b", "dosage_form": "SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69968-0459", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Extra Strength Itch Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/mL"}, {"name": "ZINC ACETATE", "strength": "1 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190601", "listing_expiration_date": "20261231"}