Package 37000-951-24
Brand: vicks sinex severe all in one sinus mucus
Generic: acetaminophen, phenylephrine hcl, guaifenesinPackage Facts
Identity
Package NDC
37000-951-24
Digits Only
3700095124
Product NDC
37000-951
Description
2 BLISTER PACK in 1 CARTON (37000-951-24) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
vicks sinex severe all in one sinus mucus
Generic
acetaminophen, phenylephrine hcl, guaifenesin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "436aef33-2f57-2401-e063-6294a90a579b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["2049223"], "spl_set_id": ["9a106291-edda-2135-e053-2995a90a44fd"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (37000-951-24) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "37000-951-24", "marketing_start_date": "20180710"}], "brand_name": "Vicks Sinex Severe All in One Sinus Mucus", "product_id": "37000-951_436aef33-2f57-2401-e063-6294a90a579b", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "37000-951", "generic_name": "Acetaminophen, Phenylephrine HCl, Guaifenesin", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Vicks Sinex Severe", "brand_name_suffix": "All in One Sinus Mucus", "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": "20180710", "listing_expiration_date": "20261231"}