Package 30142-828-09

Brand: sinus relief pressure and pain

Generic: acetaminophen, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 30142-828-09
Digits Only 3014282809
Product NDC 30142-828
Product ID 30142-828_d29c046f-2dac-42cf-815d-ca323fd3c367
Description

2 BLISTER PACK in 1 CARTON (30142-828-09) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2027-12-31
Brand sinus relief pressure and pain
Generic acetaminophen, guaifenesin, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Sinus Relief Pressure and Pain ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d29c046f-2dac-42cf-815d-ca323fd3c367", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["98de5cff-3ff5-49b0-bef9-5b9ebb86491e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (30142-828-09)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "30142-828-09", "marketing_end_date": "20271231", "marketing_start_date": "20190603"}], "brand_name": "Sinus Relief Pressure and Pain", "product_id": "30142-828_d29c046f-2dac-42cf-815d-ca323fd3c367", "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": "30142-828", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Relief Pressure and Pain", "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_end_date": "20271231", "marketing_start_date": "20190603"}