Package 37000-951-24

Brand: vicks sinex severe all in one sinus mucus

Generic: acetaminophen, phenylephrine hcl, guaifenesin
NDC Package

Package 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
Marketed Since 2018-07-10
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"}