Package 0067-6801-02

Brand: theraflu severe cold relief nighttime

Generic: acetaminophen, diphenhydramine hydrochloride, phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0067-6801-02
Digits Only 0067680102
Product NDC 0067-6801
Description

6 POWDER in 1 CARTON (0067-6801-02)

Marketing

Marketing Status
Marketed Since 2022-01-20
Brand theraflu severe cold relief nighttime
Generic acetaminophen, diphenhydramine hydrochloride, phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "132cdb61-2615-2863-e063-6394a90a7e5a", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1659175"], "spl_set_id": ["0d3b1bea-e2ca-4e07-8ae5-60627d230c96"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 POWDER in 1 CARTON (0067-6801-02)", "package_ndc": "0067-6801-02", "marketing_start_date": "20220120"}], "brand_name": "Theraflu Severe Cold relief Nighttime", "product_id": "0067-6801_132cdb61-2615-2863-e063-6394a90a7e5a", "dosage_form": "POWDER", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0067-6801", "generic_name": "Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine Hydrochloride", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Severe Cold relief Nighttime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 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": "20220120", "listing_expiration_date": "20261231"}