Package 66715-6744-9

Brand: daytime sinus severe

Generic: acetaminophen, guaifenesin, phenylephrine hcl tablet, film-coated
NDC Package

Package Facts

Identity

Package NDC 66715-6744-9
Digits Only 6671567449
Product NDC 66715-6744
Description

12 BLISTER PACK in 1 CARTON (66715-6744-9) / 2 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-08-02
Brand daytime sinus severe
Generic acetaminophen, guaifenesin, phenylephrine hcl tablet, film-coated
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0c8e6ff3-c03e-4de8-e063-6394a90a127d", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["e79d92d2-d73c-d44f-e053-2995a90a03d9"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Lil' Drug Store Products, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BLISTER PACK in 1 CARTON (66715-6744-9)  / 2 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "66715-6744-9", "marketing_start_date": "20220802"}], "brand_name": "Daytime Sinus Severe", "product_id": "66715-6744_0c8e6ff3-c03e-4de8-e063-6394a90a127d", "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": "66715-6744", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl tablet, film-coated", "labeler_name": "Lil' Drug Store Products, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime 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": "20220802", "listing_expiration_date": "20261231"}