Package 51316-927-08
Brand: severe sinus pain and congestion
Generic: acetaminophen, guaifenesin, phenylephrine hclPackage Facts
Identity
Package NDC
51316-927-08
Digits Only
5131692708
Product NDC
51316-927
Description
2 BLISTER PACK in 1 CARTON (51316-927-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
severe sinus pain and congestion
Generic
acetaminophen, guaifenesin, phenylephrine hcl
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "28869b0e-4d34-4c37-b116-b432c9c39aa3", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["fbc541ac-9465-4296-bb1e-811b9d811f40"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (51316-927-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "51316-927-08", "marketing_start_date": "20251003"}], "brand_name": "Severe Sinus Pain and Congestion", "product_id": "51316-927_28869b0e-4d34-4c37-b116-b432c9c39aa3", "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": "51316-927", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Sinus Pain and Congestion", "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": "20251003", "listing_expiration_date": "20261231"}