Package 67091-349-24
Brand: nasal decongestant pe and pain relief plus mucus relief
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
67091-349-24
Digits Only
6709134924
Product NDC
67091-349
Description
2 BLISTER PACK in 1 CARTON (67091-349-24) / 12 TABLET, COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
nasal decongestant pe and pain relief plus mucus relief
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": "2860d8a0-4862-9d45-e063-6294a90af22e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0070552250680"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["31531f90-8933-46ab-b722-cb63e7738639"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Winco Foods, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (67091-349-24) / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "67091-349-24", "marketing_start_date": "20171025"}], "brand_name": "Nasal Decongestant PE and Pain Relief Plus Mucus Relief", "product_id": "67091-349_2860d8a0-4862-9d45-e063-6294a90af22e", "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": "67091-349", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Winco Foods, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nasal Decongestant PE and Pain Relief Plus Mucus Relief", "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": "20171025", "listing_expiration_date": "20261231"}