pain reliever pm extra strength

Generic: acetaminophen, diphenhydramine hcl

Labeler: strategic sourcing services llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain reliever pm extra strength
Generic Name acetaminophen, diphenhydramine hcl
Labeler strategic sourcing services llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Strategic Sourcing Services LLC

Identifiers & Regulatory

Product NDC 62011-0256
Product ID 62011-0256_586410da-591f-4f5b-a167-4c13f136ed5c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2015-07-31
Marketing End 2026-12-31

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 620110256
Hyphenated Format 62011-0256

Supplemental Identifiers

RxCUI
1092189
UPC
0052569138991
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 extra strength (source: ndc)
Generic Name acetaminophen, diphenhydramine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (62011-0256-1) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

62011-0256-1 1 BOTTLE, PLASTIC in 1 BOX (62011-0256-1) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

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

Linked Drug Pages (1)

Pain Reliever PM Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "586410da-591f-4f5b-a167-4c13f136ed5c", "openfda": {"upc": ["0052569138991"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["3314b174-d5bb-4843-9288-9b9c5fce79d5"], "manufacturer_name": ["Strategic Sourcing Services LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (62011-0256-1)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "62011-0256-1", "marketing_end_date": "20261231", "marketing_start_date": "20150731"}], "brand_name": "Pain Reliever PM Extra Strength", "product_id": "62011-0256_586410da-591f-4f5b-a167-4c13f136ed5c", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "62011-0256", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "Strategic Sourcing Services LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever PM", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20150731"}