Package 0067-0101-06

Brand: theraflu severe cold relief nighttime

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 0067-0101-06
Digits Only 0067010106
Product NDC 0067-0101
Description

6 PACKET in 1 CARTON (0067-0101-06) / 1 POWDER, FOR SOLUTION in 1 PACKET

Marketing

Marketing Status
Marketed Since 2023-12-01
Brand theraflu severe cold relief nighttime
Generic acetaminophen, diphenhydramine hcl
Sample Package No

Linked Drug Pages (3)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "132abfab-e435-15af-e063-6294a90a6901", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["2670677"], "spl_set_id": ["14e38ef0-a5e7-4df7-824f-f27bef664d25"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 PACKET in 1 CARTON (0067-0101-06)  / 1 POWDER, FOR SOLUTION in 1 PACKET", "package_ndc": "0067-0101-06", "marketing_start_date": "20231201"}], "brand_name": "Theraflu Severe Cold Relief Nighttime", "product_id": "0067-0101_132abfab-e435-15af-e063-6294a90a6901", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0067-0101", "generic_name": "ACETAMINOPHEN, DIPHENHYDRAMINE HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Severe Cold Relief Nighttime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231201", "listing_expiration_date": "20261231"}