alka-seltzer plus severe cold powerfast fizz

Generic: aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate, doxylamine succinate

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
Generic Name aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate, doxylamine succinate
Labeler bayer healthcare llc.
Dosage Form KIT
Routes
ORAL
Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-0025
Product ID 0280-0025_45238060-730e-31e3-e063-6394a90a0841
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2020-04-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02800025
Hyphenated Format 0280-0025

Supplemental Identifiers

RxCUI
1536498 1536503 1730187
UPC
0016500587583

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 (source: ndc)
Generic Name aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate, doxylamine succinate (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 7.8 mg
  • 500 mg
  • 6.25 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (0280-0025-01) * 12 TABLET, EFFERVESCENT in 1 CARTON * 8 TABLET, EFFERVESCENT in 1 CARTON
source: ndc

Packages (1)

0280-0025-01 1 KIT in 1 CARTON (0280-0025-01) * 12 TABLET, EFFERVESCENT in 1 CARTON * 8 TABLET, EFFERVESCENT in 1 CARTON

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

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

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45238060-730e-31e3-e063-6394a90a0841", "openfda": {"upc": ["0016500587583"], "rxcui": ["1536498", "1536503", "1730187"], "spl_set_id": ["a37c9d9d-52db-23ff-e053-2995a90a8f76"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0280-0025-01)  *  12 TABLET, EFFERVESCENT in 1 CARTON *  8 TABLET, EFFERVESCENT in 1 CARTON", "package_ndc": "0280-0025-01", "marketing_start_date": "20200401"}], "brand_name": "Alka-Seltzer Plus Severe Cold PowerFast Fizz", "product_id": "0280-0025_45238060-730e-31e3-e063-6394a90a0841", "dosage_form": "KIT", "product_ndc": "0280-0025", "generic_name": "aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate, doxylamine succinate", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Severe Cold PowerFast Fizz", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200401", "listing_expiration_date": "20261231"}