pain relief pm

Generic: acetaminophen pm

Labeler: velocity pharma
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH NOT FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief pm
Generic Name acetaminophen pm
Labeler velocity pharma
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Velocity Pharma

Identifiers & Regulatory

Product NDC 76168-119
Product ID 76168-119_6c30260f-b9e7-58c3-e053-2991aa0a818c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH NOT FINAL
Application Number part343
Listing Expiration 2026-12-31
Marketing Start 2012-12-05

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 76168119
Hyphenated Format 76168-119

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 pm (source: ndc)
Application Number part343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 50 CARTON in 1 BOTTLE (76168-119-25) / 1 TABLET in 1 CARTON
source: ndc

Packages (1)

76168-119-25 50 CARTON in 1 BOTTLE (76168-119-25) / 1 TABLET in 1 CARTON

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": "6c30260f-b9e7-58c3-e053-2991aa0a818c", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["c1c1de91-6a54-4d91-93a9-b6be6d7c7dfb"], "manufacturer_name": ["Velocity Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CARTON in 1 BOTTLE (76168-119-25)  / 1 TABLET in 1 CARTON", "package_ndc": "76168-119-25", "marketing_start_date": "20180514"}], "brand_name": "Pain Relief PM", "product_id": "76168-119_6c30260f-b9e7-58c3-e053-2991aa0a818c", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "76168-119", "generic_name": "Acetaminophen PM", "labeler_name": "Velocity Pharma", "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": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20121205", "listing_expiration_date": "20261231"}