Package 63941-167-02

Brand: mucus relief sinus severe congestion relief

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63941-167-02
Digits Only 6394116702
Product NDC 63941-167
Description

2 BLISTER PACK in 1 CARTON (63941-167-02) / 10 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2028-02-28
Brand mucus relief sinus severe congestion relief
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": "45b20a26-eb43-6a1e-e063-6394a90a1bb9", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["2e751d67-51b4-4b74-a9e8-7f3bc5636984"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["VALU MERCHANDISERS COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (63941-167-02)  / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "63941-167-02", "marketing_end_date": "20280228", "marketing_start_date": "20141113"}], "brand_name": "Mucus Relief Sinus Severe Congestion Relief", "product_id": "63941-167_45b20a26-eb43-6a1e-e063-6394a90a1bb9", "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": "63941-167", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "VALU MERCHANDISERS COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Sinus Severe Congestion Relief", "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_end_date": "20280228", "marketing_start_date": "20141113"}