Package 0280-0035-01

Brand: alka-seltzer plus cough, mucus and congestion day and night powermax

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

Package Facts

Identity

Package NDC 0280-0035-01
Digits Only 0280003501
Product NDC 0280-0035
Product ID 0280-0035_4523aa8a-0db4-5337-e063-6394a90a8bda
Description

1 KIT in 1 CARTON (0280-0035-01) * 3 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 3 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2020-06-01
Brand alka-seltzer plus cough, mucus and congestion day and night powermax
Generic acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Alka-Seltzer Plus Cough, Mucus and Congestion Day and Night Powermax ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4523aa8a-0db4-5337-e063-6394a90a8bda", "openfda": {"upc": ["0016500584223"], "rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["a68df74d-dd26-3ae9-e053-2995a90a08d6"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0280-0035-01)  *  3 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  3 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-0035-01", "marketing_start_date": "20200601"}], "brand_name": "Alka-Seltzer Plus Cough, Mucus and Congestion Day and Night Powermax", "product_id": "0280-0035_4523aa8a-0db4-5337-e063-6394a90a8bda", "dosage_form": "KIT", "product_ndc": "0280-0035", "generic_name": "acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Cough, Mucus and Congestion Day and Night Powermax", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}