Package 69842-786-02

Brand: mucus relief sinus severe congestion and pain

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69842-786-02
Digits Only 6984278602
Product NDC 69842-786
Description

2 BLISTER PACK in 1 CARTON (69842-786-02) / 10 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-07-31
Brand mucus relief sinus 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": "243446a3-1648-76e1-e063-6294a90a94f8", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0050428332351"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["a0712040-48c3-cd22-e053-2995a90afa69"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (69842-786-02)  / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "69842-786-02", "marketing_end_date": "20260731", "marketing_start_date": "20200901"}], "brand_name": "Mucus Relief Sinus Severe Congestion and Pain", "product_id": "69842-786_243446a3-1648-76e1-e063-6294a90a94f8", "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": "69842-786", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Sinus 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_end_date": "20260731", "marketing_start_date": "20200901"}