Package 0067-6801-02
Brand: theraflu severe cold relief nighttime
Generic: acetaminophen, diphenhydramine hydrochloride, phenylephrine hydrochloridePackage 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
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"}