NDC 0280-1550

Alka-Seltzer Plus Cold Day and Night

Aspirin, Dextromethorphan Hydrobromide, Phenylephrine Bitartrate, Doxylamine Succinate

Alka-Seltzer Plus Cold Day and Night is a Oral Kit in the Human Otc Drug category. It is labeled and distributed by Bayer Healthcare Llc.. The primary component is .

Product ID0280-1550_75894849-a0bb-57be-e053-2a91aa0a049a
NDC0280-1550
Product TypeHuman Otc Drug
Proprietary NameAlka-Seltzer Plus Cold Day and Night
Generic NameAspirin, Dextromethorphan Hydrobromide, Phenylephrine Bitartrate, Doxylamine Succinate
Dosage FormKit
Route of AdministrationORAL
Marketing Start Date2018-09-14
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameBayer HealthCare LLC.
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0280-1550-20

1 KIT in 1 CARTON (0280-1550-20) * 6 POUCH in 1 CARTON > 2 TABLET, EFFERVESCENT in 1 POUCH * 4 POUCH in 1 CARTON > 2 TABLET, EFFERVESCENT in 1 POUCH
Marketing Start Date2018-09-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0280-1550-20 [00280155020]

Alka-Seltzer Plus Cold Day and Night KIT
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-14

Drug Details

OpenFDA Data

SPL SET ID:75894849-a0ba-57be-e053-2a91aa0a049a
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 1730187
  • 1536503
  • 1536498
  • UPC Code
  • 0016500572633
  • NDC Crossover Matching brand name "Alka-Seltzer Plus Cold Day and Night" or generic name "Aspirin, Dextromethorphan Hydrobromide, Phenylephrine Bitartrate, Doxylamine Succinate"

    NDCBrand NameGeneric Name
    0280-1550Alka-Seltzer Plus Cold Day and NightAspirin, Dextromethorphan hydrobromide, Phenylephrine bitartrate, Doxylamine succinate
    0280-0025Alka-Seltzer Plus Severe Cold PowerFast Fizzaspirin, dextromethorphan hydrobromide, phenylephrine bitartrate, doxylamine succinate

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