0280-0069 : Alka-seltzer Plus Severe Cold Powerfast Fizz Day and NightAlka-seltzer Plus Severe Cold Powerfast Fizz Day and Night Oral Kit


NDC: 0280-0069
Labeler: Bayer Healthcare LLC.
Product Type: Human OTC Drug
Drug Name: Alka-seltzer Plus Severe Cold Powerfast Fizz Day and Night
Dosage Form: Oral Kit
Application #: part341
Rev. Date: 


NDC Package Codes:

  • 0280-0069-01: 1 KIT IN 1 CARTON (0280‑0069‑01) * 1 TABLET, EFFERVESCENT IN 1 POUCH * 1 TABLET, EFFERVESCENT IN 1 POUCH

Related Products:

Based on records with the same trade name.
  • 0280-0086 Alka-seltzer Plus Severe Cold Powerfast Fizz Day and NightAlka-seltzer Plus Severe Cold Powerfast Fizz Day and Night Oral Kit by Bayer Healthcare LLC.
  • 0280-0109 Alka-seltzer Plus Severe Cold Powerfast Fizz Day and NightAlka-seltzer Plus Severe Cold Powerfast Fizz Day and Night Oral Kit by Bayer Healthcare LLC.
  • 0280-0110 Alka-seltzer Plus Severe Cold Powerfast Fizz Day and NightAlka-seltzer Plus Severe Cold Powerfast Fizz Day and Night Oral Kit by Bayer Healthcare LLC.

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.