Package 0067-8212-01

Brand: theraflu severe cold relief nighttime with honey elderberry flavor

Generic: acetaminophen, diphenhydramine hcl, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 0067-8212-01
Digits Only 0067821201
Product NDC 0067-8212
Product ID 0067-8212_132a7bfc-7f1c-8436-e063-6394a90a5238
Description

6 PACKET in 1 CARTON (0067-8212-01) / 1 POWDER, FOR SOLUTION in 1 PACKET

Marketing

Marketing Status
Marketed Since 2023-05-01
Brand theraflu severe cold relief nighttime with honey elderberry flavor
Generic acetaminophen, diphenhydramine hcl, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Theraflu Severe Cold Relief Nighttime with Honey Elderberry Flavor ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "132a7bfc-7f1c-8436-e063-6394a90a5238", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1659960"], "spl_set_id": ["d4ce06aa-776f-45e4-a1a6-9cf13797048f"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 PACKET in 1 CARTON (0067-8212-01)  / 1 POWDER, FOR SOLUTION in 1 PACKET", "package_ndc": "0067-8212-01", "marketing_start_date": "20230501"}], "brand_name": "Theraflu Severe Cold Relief Nighttime with Honey Elderberry Flavor", "product_id": "0067-8212_132a7bfc-7f1c-8436-e063-6394a90a5238", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0067-8212", "generic_name": "ACETAMINOPHEN, DIPHENHYDRAMINE HCl, PHENYLEPHRINE HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu", "brand_name_suffix": "Severe Cold Relief Nighttime with Honey Elderberry Flavor", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230501", "listing_expiration_date": "20261231"}