benadryl extra strength itch stopping

Generic: diphenhydramine hydrochloride

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

Drug Facts

Product Profile

Brand Name benadryl extra strength itch stopping
Generic Name diphenhydramine hydrochloride
Labeler kenvue brands llc
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

diphenhydramine hydrochloride 20 mg/mL

Manufacturer
Kenvue Brands LLC

Identifiers & Regulatory

Product NDC 69968-0242
Product ID 69968-0242_33854b34-d15c-96fa-e063-6394a90ac610
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2013-10-01

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 699680242
Hyphenated Format 69968-0242

Supplemental Identifiers

RxCUI
1049880 1049882
UPC
0312547171571
UNII
TC2D6JAD40

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 stopping (source: ndc)
Generic Name diphenhydramine hydrochloride (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 103 mL in 1 TUBE (69968-0242-3)
source: ndc

Packages (1)

69968-0242-3 103 mL in 1 TUBE (69968-0242-3)

Ingredients (1)

diphenhydramine hydrochloride (20 mg/mL)

Linked Drug Pages (1)

Benadryl Extra Strength Itch Stopping ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "33854b34-d15c-96fa-e063-6394a90ac610", "openfda": {"upc": ["0312547171571"], "unii": ["TC2D6JAD40"], "rxcui": ["1049880", "1049882"], "spl_set_id": ["66a2fd60-1757-45cc-a195-ecb9241dca2a"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "103 mL in 1 TUBE (69968-0242-3)", "package_ndc": "69968-0242-3", "marketing_start_date": "20131001"}], "brand_name": "Benadryl Extra Strength Itch Stopping", "product_id": "69968-0242_33854b34-d15c-96fa-e063-6394a90ac610", "dosage_form": "GEL", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69968-0242", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Extra Strength Itch Stopping", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20131001", "listing_expiration_date": "20261231"}