extra strength pain reliever pm

Generic: acetaminophen, diphenhydramine hcl

Labeler: ingles markets, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength pain reliever pm
Generic Name acetaminophen, diphenhydramine hcl
Labeler ingles markets, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
INGLES MARKETS, INC.

Identifiers & Regulatory

Product NDC 62936-0224
Product ID 62936-0224_27fd4de9-1f9c-86ef-e063-6394a90abf75
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2024-07-01

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 629360224
Hyphenated Format 62936-0224

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 extra strength pain reliever pm (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 in 1 CARTON (62936-0224-1) / 50 TABLET in 1 BOTTLE
source: ndc

Packages (1)

62936-0224-1 1 BOTTLE in 1 CARTON (62936-0224-1) / 50 TABLET in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

Extra Strength Pain Reliever PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "27fd4de9-1f9c-86ef-e063-6394a90abf75", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["27fd288e-c07a-617f-e063-6394a90a17a4"], "manufacturer_name": ["INGLES MARKETS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (62936-0224-1)  / 50 TABLET in 1 BOTTLE", "package_ndc": "62936-0224-1", "marketing_start_date": "20240701"}], "brand_name": "Extra Strength Pain Reliever PM", "product_id": "62936-0224_27fd4de9-1f9c-86ef-e063-6394a90abf75", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "62936-0224", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "INGLES MARKETS, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Pain Reliever 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": "20240701", "listing_expiration_date": "20261231"}