pain relief pm

Generic: acetaminophen and diphenhydramine hydrochloride

Labeler: hyvee inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief pm
Generic Name acetaminophen and diphenhydramine hydrochloride
Labeler hyvee inc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
HYVEE INC

Identifiers & Regulatory

Product NDC 42507-095
Product ID 42507-095_440cb853-1454-0cda-e063-6294a90a73a1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2025-10-22

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 42507095
Hyphenated Format 42507-095

Supplemental Identifiers

RxCUI
1092189
UPC
0075450825930
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 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 (42507-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 225 TABLET, COATED in 1 BOTTLE, PLASTIC (42507-095-17)
source: ndc

Packages (2)

42507-095-03 1 BOTTLE, PLASTIC in 1 CARTON (42507-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 42507-095-17 225 TABLET, COATED in 1 BOTTLE, PLASTIC (42507-095-17)

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": "440cb853-1454-0cda-e063-6294a90a73a1", "openfda": {"upc": ["0075450825930"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["3e60703b-a5cf-333a-e063-6394a90a2087"], "manufacturer_name": ["HYVEE INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (42507-095-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "42507-095-03", "marketing_start_date": "20251022"}, {"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE, PLASTIC (42507-095-17)", "package_ndc": "42507-095-17", "marketing_start_date": "20251120"}], "brand_name": "Pain Relief PM", "product_id": "42507-095_440cb853-1454-0cda-e063-6294a90a73a1", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "42507-095", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "HYVEE INC", "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": "20251022", "listing_expiration_date": "20261231"}