Package 0067-6800-02

Brand: theraflu severe cold relief daytime berry burst

Generic: acetaminophen, dextromethorphan hbr, phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0067-6800-02
Digits Only 0067680002
Product NDC 0067-6800
Product ID 0067-6800_77b6db34-5ac4-46a5-9d6d-1c4cc83a9ba9
Description

6 POWDER in 1 CARTON (0067-6800-02)

Marketing

Marketing Status
Marketed Since 2022-01-20
Brand theraflu severe cold relief daytime berry burst
Generic acetaminophen, dextromethorphan hbr, phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Theraflu Severe Cold Relief Daytime Berry Burst ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "77b6db34-5ac4-46a5-9d6d-1c4cc83a9ba9", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1659967"], "spl_set_id": ["ebbb2f4b-ba84-40ad-96f6-60225119a33b"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 POWDER in 1 CARTON (0067-6800-02)", "package_ndc": "0067-6800-02", "marketing_start_date": "20220120"}], "brand_name": "Theraflu Severe Cold Relief Daytime Berry Burst", "product_id": "0067-6800_77b6db34-5ac4-46a5-9d6d-1c4cc83a9ba9", "dosage_form": "POWDER", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0067-6800", "generic_name": "Acetaminophen, Dextromethorphan HBr, Phenylephrine Hydrochloride", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Severe Cold Relief Daytime Berry Burst", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 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"}