alka-seltzer plus severe cold powerfast fizz day and night

Generic: aspirin, chlorpheniramine maleate, 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, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine bitartrate
Labeler bayer healthcare llc.
Dosage Form KIT
Routes
ORAL
Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-0109
Product ID 0280-0109_47e3199f-608e-3107-e063-6294a90abdb1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2027-12-31
Marketing Start 2021-08-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02800109
Hyphenated Format 0280-0109

Supplemental Identifiers

RxCUI
1536498 1537029 2664074
UPC
0016500598879

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, chlorpheniramine maleate, 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
  • 2 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (0280-0109-01) * 2 TABLET, EFFERVESCENT in 1 POUCH * 2 TABLET, EFFERVESCENT in 1 POUCH
source: ndc

Packages (1)

0280-0109-01 1 KIT in 1 CARTON (0280-0109-01) * 2 TABLET, EFFERVESCENT in 1 POUCH * 2 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": "47e3199f-608e-3107-e063-6294a90abdb1", "openfda": {"upc": ["0016500598879"], "rxcui": ["1536498", "1537029", "2664074"], "spl_set_id": ["fc60af2f-83cb-99ea-e053-6394a90a0b3b"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0280-0109-01)  *  2 TABLET, EFFERVESCENT in 1 POUCH *  2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "0280-0109-01", "marketing_start_date": "20210805"}], "brand_name": "Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and Night", "product_id": "0280-0109_47e3199f-608e-3107-e063-6294a90abdb1", "dosage_form": "KIT", "product_ndc": "0280-0109", "generic_name": "aspirin, chlorpheniramine maleate, 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": "20271231"}