Package 49035-586-04

Brand: day severe cold and night cold and flu maximum strength

Generic: acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 49035-586-04
Digits Only 4903558604
Product NDC 49035-586
Product ID 49035-586_2778b43d-a097-6f74-e063-6294a90a2cd2
Description

1 KIT in 1 CARTON (49035-586-04) * 2 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-01-31
Brand day severe cold and night cold and flu maximum strength
Generic acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Day Severe Cold and Night Cold and Flu Maximum Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "2778b43d-a097-6f74-e063-6294a90a2cd2", "openfda": {"rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["7492b381-9eca-4b07-b356-63fdaea14f81"], "manufacturer_name": ["Wal-Mart Stores, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (49035-586-04)  *  2 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  1 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "49035-586-04", "marketing_start_date": "20180131"}], "brand_name": "Day Severe Cold and Night Cold and Flu Maximum Strength", "product_id": "49035-586_2778b43d-a097-6f74-e063-6294a90a2cd2", "dosage_form": "KIT", "product_ndc": "49035-586", "generic_name": "acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride", "labeler_name": "Wal-Mart Stores, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Day Severe Cold and Night Cold and Flu", "brand_name_suffix": "Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180131", "listing_expiration_date": "20261231"}