Package 67751-239-02
Brand: tylenol sinus severe
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
67751-239-02
Digits Only
6775123902
Product NDC
67751-239
Description
2 POUCH in 1 CARTON (67751-239-02) / 2 TABLET, COATED in 1 POUCH
Marketing
Marketing Status
Brand
tylenol sinus severe
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": "435b5b96-73d0-4d01-e063-6394a90ae4dd", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["435b4a2a-d6bf-ec25-e063-6294a90a3f06"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (67751-239-01) / 2 TABLET, COATED in 1 POUCH", "package_ndc": "67751-239-01", "marketing_start_date": "20250219"}, {"sample": false, "description": "2 POUCH in 1 CARTON (67751-239-02) / 2 TABLET, COATED in 1 POUCH", "package_ndc": "67751-239-02", "marketing_start_date": "20250219"}], "brand_name": "Tylenol Sinus Severe", "product_id": "67751-239_435b5b96-73d0-4d01-e063-6394a90ae4dd", "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": "67751-239", "generic_name": "Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride", "labeler_name": "Navajo Manufacturing Company Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tylenol Sinus 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": "20250219", "listing_expiration_date": "20261231"}