Package 11673-286-01

Brand: maximum strength daytime cold and flu and nighttime severe cold and flu

Generic: acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride,triprolidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 11673-286-01
Digits Only 1167328601
Product NDC 11673-286
Description

1 KIT in 1 CARTON (11673-286-01) * 180 mL in 1 BOTTLE (11673-872-03) * 180 mL in 1 BOTTLE (11673-295-03)

Marketing

Marketing Status
Marketed Since 2024-05-01
Brand maximum strength daytime cold and flu and nighttime severe cold and flu
Generic acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride,triprolidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "203f3d03-46d9-3747-e063-6294a90a251e", "openfda": {"upc": ["0311673286012"], "rxcui": ["1116572", "2173662", "2637727"], "spl_set_id": ["0fc523ce-55a7-6384-e063-6394a90aad3f"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (11673-286-01)  *  180 mL in 1 BOTTLE (11673-872-03)  *  180 mL in 1 BOTTLE (11673-295-03)", "package_ndc": "11673-286-01", "marketing_start_date": "20240501"}], "brand_name": "Maximum Strength Daytime Cold and Flu and Nighttime Severe Cold and Flu", "product_id": "11673-286_203f3d03-46d9-3747-e063-6294a90a251e", "dosage_form": "KIT", "product_ndc": "11673-286", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, and Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride,Triprolidine Hydrochloride", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum Strength Daytime Cold and Flu and Nighttime Severe Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}