Package 0067-0112-01

Brand: theraflu severe cold relief nighttime soft chews

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 0067-0112-01
Digits Only 0067011201
Product NDC 0067-0112
Description

20 TABLET, CHEWABLE in 1 BOTTLE (0067-0112-01)

Marketing

Marketing Status
Marketed Since 2024-09-30
Brand theraflu severe cold relief nighttime soft chews
Generic acetaminophen, diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "21636332-818b-26bf-e063-6394a90a1925", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["2691689"], "spl_set_id": ["6ba64bbe-7599-406a-9187-737c0f8c1c2a"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, CHEWABLE in 1 BOTTLE (0067-0112-01)", "package_ndc": "0067-0112-01", "marketing_start_date": "20240930"}], "brand_name": "Theraflu Severe Cold Relief Nighttime Soft Chews", "product_id": "0067-0112_21636332-818b-26bf-e063-6394a90a1925", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0067-0112", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu", "brand_name_suffix": "Severe Cold Relief Nighttime Soft Chews", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240930", "listing_expiration_date": "20261231"}