benadryl

Generic: diphenhydramine hydrochloride

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

Drug Facts

Product Profile

Brand Name benadryl
Generic Name diphenhydramine hydrochloride
Labeler kenvue brands llc
Dosage Form KIT
Manufacturer
Kenvue Brands LLC

Identifiers & Regulatory

Product NDC 50580-370
Product ID 50580-370_21716a1f-3636-bdde-e063-6394a90aab01
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2017-06-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50580370
Hyphenated Format 50580-370

Supplemental Identifiers

RxCUI
1049630 1049632

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 (source: ndc)
Generic Name diphenhydramine hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 25 mg
source: label
Packaging
  • 1 KIT in 1 PACKAGE (50580-370-01) * 1 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE * 4 BLISTER PACK in 1 CARTON / 12 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "21716a1f-3636-bdde-e063-6394a90aab01", "openfda": {"rxcui": ["1049630", "1049632"], "spl_set_id": ["2884d2dc-2d4a-4ca6-ab73-688a80b428eb"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE (50580-370-01)  *  1 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE *  4 BLISTER PACK in 1 CARTON / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-370-01", "marketing_start_date": "20170612"}], "brand_name": "Benadryl", "product_id": "50580-370_21716a1f-3636-bdde-e063-6394a90aab01", "dosage_form": "KIT", "product_ndc": "50580-370", "generic_name": "diphenhydramine hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170612", "listing_expiration_date": "20261231"}