Package 49035-527-08
Brand: sinus congestion and pain severe
Generic: acetaminophen, guaifenesin and phenylephrine hclPackage Facts
Identity
Package NDC
49035-527-08
Digits Only
4903552708
Product NDC
49035-527
Description
2 BLISTER PACK in 1 CARTON (49035-527-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
sinus congestion and pain severe
Generic
acetaminophen, guaifenesin and phenylephrine hcl
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dbfccbf6-2f75-4679-824d-f8cdfd7b7319", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0681131187206"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["f51d1d52-39c2-4259-8b30-f9ac21edb265"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Wal-Mart Stores Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (49035-527-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "49035-527-08", "marketing_start_date": "20050806"}], "brand_name": "Sinus Congestion and Pain Severe", "product_id": "49035-527_dbfccbf6-2f75-4679-824d-f8cdfd7b7319", "dosage_form": "TABLET, FILM 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": "49035-527", "generic_name": "Acetaminophen, Guaifenesin and Phenylephrine HCl", "labeler_name": "Wal-Mart Stores Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Congestion and Pain", "brand_name_suffix": "Severe", "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": "20050806", "listing_expiration_date": "20261231"}