Package 0067-6803-02

Brand: theraflu severe cold relief nighttime

Generic: acetaminophen, diphenhydramine hcl, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 0067-6803-02
Digits Only 0067680302
Product NDC 0067-6803
Product ID 0067-6803_10682cca-1329-1e41-e063-6394a90a7e21
Description

6 PACKET in 1 CARTON (0067-6803-02) / 237 mL in 1 PACKET

Marketing

Marketing Status
Marketed Since 2023-01-20
Brand theraflu severe cold relief nighttime
Generic acetaminophen, diphenhydramine hcl, phenylephrine hcl
Sample Package No

Linked Drug Pages (2)

Theraflu Severe Cold Relief Daytime and Theraflu Severe Cold Relief Nighttime ndc-match (0.95) Theraflu Severe Cold Relief Nighttime ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "10682cca-1329-1e41-e063-6394a90a7e21", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1659960"], "spl_set_id": ["4daca846-8511-4303-9e6c-9469f7f260ba"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 PACKET in 1 CARTON (0067-6803-02)  / 237 mL in 1 PACKET", "package_ndc": "0067-6803-02", "marketing_start_date": "20230120"}], "brand_name": "Theraflu Severe Cold Relief Nighttime", "product_id": "0067-6803_10682cca-1329-1e41-e063-6394a90a7e21", "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": "0067-6803", "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", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/237mL"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/237mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/237mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230120", "listing_expiration_date": "20261231"}