pain reliever pm

Generic: acetaminophen, diphenhydramine hcl

Labeler: target corporation
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 target corporation
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
TARGET Corporation

Identifiers & Regulatory

Product NDC 11673-754
Product ID 11673-754_71c48239-a3f8-4d86-b883-0d81a1b11894
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2023-08-01

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 11673754
Hyphenated Format 11673-754

Supplemental Identifiers

RxCUI
1092189
UPC
0359726863117
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 BOX (11673-754-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "71c48239-a3f8-4d86-b883-0d81a1b11894", "openfda": {"upc": ["0359726863117"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["1fc3806e-a5c4-4a6e-951b-dfbf9f5771f1"], "manufacturer_name": ["TARGET Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (11673-754-10)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11673-754-10", "marketing_start_date": "20230801"}], "brand_name": "Pain Reliever PM", "product_id": "11673-754_71c48239-a3f8-4d86-b883-0d81a1b11894", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "11673-754", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "TARGET Corporation", "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_start_date": "20230801", "listing_expiration_date": "20261231"}