Package 72476-167-02

Brand: severe congestion and pain

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72476-167-02
Digits Only 7247616702
Product NDC 72476-167
Description

2 BLISTER PACK in 1 CARTON (72476-167-02) / 10 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-10-01
Brand severe congestion and pain
Generic acetaminophen, guaifenesin, and phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2489f157-033a-2e9c-e063-6294a90ac70b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["8bc68a71-62c5-a04f-e053-2995a90a92fd"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Retail Business Services , LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (72476-167-02)  / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "72476-167-02", "marketing_start_date": "20191001"}], "brand_name": "Severe Congestion and Pain", "product_id": "72476-167_2489f157-033a-2e9c-e063-6294a90ac70b", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "72476-167", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Retail Business Services , LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Congestion and Pain", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191001", "listing_expiration_date": "20261231"}