alka-seltzer plus severe cold powerfast fizz day and night

Generic: aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate

Labeler: bayer healthcare llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name alka-seltzer plus severe cold powerfast fizz day and night
Generic Name aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate
Labeler bayer healthcare llc.
Dosage Form KIT
Routes
ORAL
Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-0069
Product ID 0280-0069_45264ea9-aed7-8b75-e063-6394a90a74c1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-08-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02800069
Hyphenated Format 0280-0069

Supplemental Identifiers

RxCUI
1536498 2565491 2565492
UPC
0016500594604

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name alka-seltzer plus severe cold powerfast fizz day and night (source: ndc)
Generic Name aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 7.8 mg
  • 6.25 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (0280-0069-01) * 1 TABLET, EFFERVESCENT in 1 POUCH * 1 TABLET, EFFERVESCENT in 1 POUCH
source: ndc

Packages (1)

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

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and Night ndc-match (0.9)

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"}