acetaminophen pm

Generic: acetaminophen and diphenhydramine hydrochloride

Labeler: retail business services , llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen pm
Generic Name acetaminophen and diphenhydramine hydrochloride
Labeler retail business services , llc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
RETAIL BUSINESS SERVICES , LLC.

Identifiers & Regulatory

Product NDC 72476-171
Product ID 72476-171_1adb0e1c-a806-ed20-e063-6294a90a46ee
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2024-03-01

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 72476171
Hyphenated Format 72476-171

Supplemental Identifiers

RxCUI
1092189
UPC
0341520319624
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 (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 (72476-171-01) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (72476-171-03) / 80 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

72476-171-01 1 BOTTLE, PLASTIC in 1 CARTON (72476-171-01) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC 72476-171-03 1 BOTTLE, PLASTIC in 1 CARTON (72476-171-03) / 80 TABLET, COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

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

Linked Drug Pages (1)

ACETAMINOPHEN PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1adb0e1c-a806-ed20-e063-6294a90a46ee", "openfda": {"upc": ["0341520319624"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["093199be-e92a-6f60-e063-6294a90a8533"], "manufacturer_name": ["RETAIL BUSINESS SERVICES , LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (72476-171-01)  / 20 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "72476-171-01", "marketing_start_date": "20240301"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (72476-171-03)  / 80 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "72476-171-03", "marketing_start_date": "20240301"}], "brand_name": "ACETAMINOPHEN PM", "product_id": "72476-171_1adb0e1c-a806-ed20-e063-6294a90a46ee", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72476-171", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "RETAIL BUSINESS SERVICES , LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN PM", "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": "20240301", "listing_expiration_date": "20261231"}