Package 0280-0069-01

Brand: alka-seltzer plus severe cold powerfast fizz day and night

Generic: aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate
NDC Package

Package Facts

Identity

Package NDC 0280-0069-01
Digits Only 0280006901
Product NDC 0280-0069
Description

1 KIT in 1 CARTON (0280-0069-01) * 1 TABLET, EFFERVESCENT in 1 POUCH * 1 TABLET, EFFERVESCENT in 1 POUCH

Marketing

Marketing Status
Marketed Since 2021-08-05
Brand alka-seltzer plus severe cold powerfast fizz day and night
Generic aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45264ea9-aed7-8b75-e063-6394a90a74c1", "openfda": {"upc": ["0016500594604"], "rxcui": ["1536498", "2565491", "2565492"], "spl_set_id": ["c2232241-6e57-1427-e053-2995a90a488a"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0280-0069-01)  *  1 TABLET, EFFERVESCENT in 1 POUCH *  1 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "0280-0069-01", "marketing_start_date": "20210805"}], "brand_name": "Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and Night", "product_id": "0280-0069_45264ea9-aed7-8b75-e063-6394a90a74c1", "dosage_form": "KIT", "product_ndc": "0280-0069", "generic_name": "aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and Night", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210805", "listing_expiration_date": "20261231"}