Package 72476-167-02
Brand: severe congestion and pain
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage 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
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"}