Package 0067-8129-08

Brand: theraflu expressmax nighttime severe cold and cough

Generic: acetaminophen, diphenhydramine hcl, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 0067-8129-08
Digits Only 0067812908
Product NDC 0067-8129
Product ID 0067-8129_131827e6-0141-cf1d-e063-6294a90ae248
Description

245.5 mL in 1 BOTTLE (0067-8129-08)

Marketing

Marketing Status
Marketed Since 2015-07-15
Brand theraflu expressmax nighttime severe cold and cough
Generic acetaminophen, diphenhydramine hcl, phenylephrine hcl
Sample Package No

Linked Drug Pages (2)

Theraflu ExpressMax Daytime Nighttime Value Pack ndc-match (0.95) Theraflu ExpressMax Nighttime Severe Cold and Cough ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "131827e6-0141-cf1d-e063-6294a90ae248", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1298348"], "spl_set_id": ["f5a66541-1b15-4dfe-91e0-d8d5f8fdc7fb"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "245.5 mL in 1 BOTTLE (0067-8129-08)", "package_ndc": "0067-8129-08", "marketing_start_date": "20150715"}], "brand_name": "Theraflu ExpressMax Nighttime Severe Cold and Cough", "product_id": "0067-8129_131827e6-0141-cf1d-e063-6294a90ae248", "dosage_form": "SYRUP", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0067-8129", "generic_name": "Acetaminophen, Diphenhydramine HCl, Phenylephrine HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu ExpressMax", "brand_name_suffix": "Nighttime Severe Cold and Cough", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/30mL"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/30mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/30mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150715", "listing_expiration_date": "20261231"}