pain reliever pm

Generic: acetaminophen, diphenhydramine hcl

Labeler: chain drug consortium
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain reliever pm
Generic Name acetaminophen, diphenhydramine hcl
Labeler chain drug consortium
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Chain Drug Consortium

Identifiers & Regulatory

Product NDC 68016-540
Product ID 68016-540_8877ab6d-dd8f-43d3-bd3b-20bcbc38c2f4
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Marketing Start 2023-05-12
Marketing End 2026-05-31

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 68016540
Hyphenated Format 68016-540

Supplemental Identifiers

RxCUI
1092189
UPC
0840986037344
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 pain reliever pm (source: ndc)
Generic Name acetaminophen, diphenhydramine hcl (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 (68016-540-01) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

68016-540-01 1 BOTTLE, PLASTIC in 1 CARTON (68016-540-01) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

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

Linked Drug Pages (1)

Pain Reliever PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8877ab6d-dd8f-43d3-bd3b-20bcbc38c2f4", "openfda": {"upc": ["0840986037344"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["57d7dbe2-52df-426c-b92b-9ffdb9f10e19"], "manufacturer_name": ["Chain Drug Consortium"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-540-01)  / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-540-01", "marketing_end_date": "20260531", "marketing_start_date": "20230512"}], "brand_name": "Pain Reliever PM", "product_id": "68016-540_8877ab6d-dd8f-43d3-bd3b-20bcbc38c2f4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68016-540", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "Chain Drug Consortium", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever 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_end_date": "20260531", "marketing_start_date": "20230512"}