Package 69842-786-02
Brand: mucus relief sinus severe congestion and pain
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage 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
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"}