Package 0280-0062-01

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

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

Package Facts

Identity

Package NDC 0280-0062-01
Digits Only 0280006201
Product NDC 0280-0062
Product ID 0280-0062_45263262-6498-654f-e063-6394a90a4683
Description

1 KIT in 1 CARTON (0280-0062-01) * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Marketing

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

Linked Drug Pages (1)

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

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45263262-6498-654f-e063-6394a90a4683", "openfda": {"upc": ["0016500584216"], "rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["a6b8dc25-0fb9-1823-e053-2a95a90adf93"], "manufacturer_name": ["Bayer HealthCare, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0280-0062-01)  *  2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-0062-01", "marketing_start_date": "20200601"}], "brand_name": "Alka-Seltzer Plus Maximum Strength Cough, Mucus and Congestion Day and Night", "product_id": "0280-0062_45263262-6498-654f-e063-6394a90a4683", "dosage_form": "KIT", "product_ndc": "0280-0062", "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 Maximum Strength Cough, Mucus and Congestion Day and Night", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}