Package 62936-0224-1

Brand: extra strength pain reliever pm

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 62936-0224-1
Digits Only 6293602241
Product NDC 62936-0224
Product ID 62936-0224_27fd4de9-1f9c-86ef-e063-6394a90abf75
Description

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

Marketing

Marketing Status
Marketed Since 2024-07-01
Brand extra strength pain reliever pm
Generic acetaminophen, diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Extra Strength Pain Reliever PM ndc-match (0.95)

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"}