acetaminophen pm extra strength

Generic: acetaminophen and diphenhydramine hydrochloride

Labeler: winco foods, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen pm extra strength
Generic Name acetaminophen and diphenhydramine hydrochloride
Labeler winco foods, llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1, diphenhydramine hydrochloride 25 mg/1

Manufacturer
WinCo Foods, LLC

Identifiers & Regulatory

Product NDC 67091-137
Product ID 67091-137_1cd2d784-de45-3a41-e063-6394a90aabdf
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2014-12-15

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 67091137
Hyphenated Format 67091-137

Supplemental Identifiers

RxCUI
1092189
UPC
0070552230354
UNII
362O9ITL9D 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 acetaminophen pm extra strength (source: ndc)
Generic Name acetaminophen and diphenhydramine hydrochloride (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (67091-137-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

67091-137-50 1 BOTTLE, PLASTIC in 1 CARTON (67091-137-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

acetaminophen (500 mg/1) diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Acetaminophen PM Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1cd2d784-de45-3a41-e063-6394a90aabdf", "openfda": {"upc": ["0070552230354"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["3c57498c-86b0-4ba3-881e-c742a2e8ece5"], "manufacturer_name": ["WinCo Foods, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (67091-137-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "67091-137-50", "marketing_start_date": "20141215"}], "brand_name": "Acetaminophen PM Extra Strength", "product_id": "67091-137_1cd2d784-de45-3a41-e063-6394a90aabdf", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "67091-137", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "WinCo Foods, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen PM", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20141215", "listing_expiration_date": "20261231"}