pain reliever pm extra strength (59726-868)

Drug Facts

Product Profile

Brand Name pain reliever pm extra strength

Generic Name acetaminophen diphenhydramine hcl

Labeler p & l development, llc

Dosage Form TABLET, COATED

Routes

ORAL

Active Ingredients

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

Manufacturer

P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-868

Product ID 59726-868_fd04bd61-2bce-4ec0-99b0-ebd0995d3aba

Product Type HUMAN OTC DRUG

Marketing Category OTC MONOGRAPH DRUG

Application Number M013

Marketing Start 2021-03-26

Marketing End 2026-12-26

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 59726868

Hyphenated Format 59726-868

Supplemental Identifiers

RxCUI

1092189

UPC

0359726863100

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 M013 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

500 mg/1
25 mg/1

source: ndc

Packaging

1 BOTTLE, PLASTIC in 1 BOX (59726-868-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
1 BOTTLE, PLASTIC in 1 BOX (59726-868-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
1 BOTTLE, PLASTIC in 1 BOX (59726-868-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

source: ndc

Packages (3)

59726-868-10 1 BOTTLE, PLASTIC in 1 BOX (59726-868-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 59726-868-24 1 BOTTLE, PLASTIC in 1 BOX (59726-868-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC 59726-868-50 1 BOTTLE, PLASTIC in 1 BOX (59726-868-50) / 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": "fd04bd61-2bce-4ec0-99b0-ebd0995d3aba", "openfda": {"upc": ["0359726863100"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["90eba2e8-52c3-43f5-ba93-4a520368c7f4"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-868-10)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "59726-868-10", "marketing_end_date": "20261226", "marketing_start_date": "20210326"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-868-24)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "59726-868-24", "marketing_end_date": "20261226", "marketing_start_date": "20210326"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-868-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "59726-868-50", "marketing_end_date": "20261226", "marketing_start_date": "20210326"}], "brand_name": "Pain Reliever PM extra strength", "product_id": "59726-868_fd04bd61-2bce-4ec0-99b0-ebd0995d3aba", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "59726-868", "generic_name": "Acetaminophen Diphenhydramine HCL", "labeler_name": "P & L Development, 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": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261226", "marketing_start_date": "20210326"}