pain relief pm

Generic: acetaminophen, diphenhydramine

Labeler: pioneer life sciences, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief pm
Generic Name acetaminophen, diphenhydramine
Labeler pioneer life sciences, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Pioneer Life Sciences, LLC

Identifiers & Regulatory

Product NDC 72090-032
Product ID 72090-032_3534d9ad-25c0-42ed-89d8-bc28ca3488dd
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2024-08-29

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 72090032
Hyphenated Format 72090-032

Supplemental Identifiers

RxCUI
1092189
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 relief pm (source: ndc)
Generic Name acetaminophen, diphenhydramine (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 375 TABLET in 1 BOTTLE (72090-032-01)
source: ndc

Packages (1)

72090-032-01 375 TABLET in 1 BOTTLE (72090-032-01)

Ingredients (2)

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

Linked Drug Pages (1)

Pain Relief PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3534d9ad-25c0-42ed-89d8-bc28ca3488dd", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["0181af13-da32-4431-be39-c31fdfac9202"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "375 TABLET in 1 BOTTLE (72090-032-01)", "package_ndc": "72090-032-01", "marketing_start_date": "20240829"}], "brand_name": "Pain Relief PM", "product_id": "72090-032_3534d9ad-25c0-42ed-89d8-bc28ca3488dd", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72090-032", "generic_name": "ACETAMINOPHEN, DIPHENHYDRAMINE", "labeler_name": "Pioneer Life Sciences, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief 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": "20240829", "listing_expiration_date": "20261231"}