extra strength pain relief pm (63941-095)

Drug Facts

Product Profile

Brand Name extra strength pain relief pm

Generic Name acetaminophen and diphenhydramine hydrochloride

Labeler valu merchandisers company

Dosage Form TABLET, COATED

Routes

ORAL

Active Ingredients

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

Manufacturer

VALU MERCHANDISERS COMPANY

Identifiers & Regulatory

Product NDC 63941-095

Product ID 63941-095_45b0d446-7d54-c0c8-e063-6294a90a5230

Product Type HUMAN OTC DRUG

Marketing Category OTC MONOGRAPH DRUG

Application Number M013

Marketing Start 2010-02-01

Marketing End 2028-03-31

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 63941095

Hyphenated Format 63941-095

Supplemental Identifiers

RxCUI

1092189

UPC

0070038201786

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 extra strength 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 (63941-095-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
1 BOTTLE, PLASTIC in 1 CARTON (63941-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
2 BOTTLE, PLASTIC in 1 CARTON (63941-095-09) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

source: ndc

Packages (3)

63941-095-02 1 BOTTLE, PLASTIC in 1 CARTON (63941-095-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC 63941-095-03 1 BOTTLE, PLASTIC in 1 CARTON (63941-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 63941-095-09 2 BOTTLE, PLASTIC in 1 CARTON (63941-095-09) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

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

Linked Drug Pages (1)

Extra Strength Pain Relief PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "45b0d446-7d54-c0c8-e063-6294a90a5230", "openfda": {"upc": ["0070038201786"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["f8820150-feec-4062-85bb-14525ddf691f"], "manufacturer_name": ["VALU MERCHANDISERS COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-095-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-095-02", "marketing_end_date": "20271031", "marketing_start_date": "20100201"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-095-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-095-03", "marketing_end_date": "20271231", "marketing_start_date": "20111004"}, {"sample": false, "description": "2 BOTTLE, PLASTIC in 1 CARTON (63941-095-09)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-095-09", "marketing_end_date": "20280331", "marketing_start_date": "20120203"}], "brand_name": "Extra Strength Pain Relief PM", "product_id": "63941-095_45b0d446-7d54-c0c8-e063-6294a90a5230", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63941-095", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "VALU MERCHANDISERS COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength 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_end_date": "20280331", "marketing_start_date": "20100201"}