NDC 0280-0221

Alka-Seltzer Heartburn ReliefChews

Calcium Carbonate

Alka-Seltzer Heartburn ReliefChews is a Oral Tablet, Chewable in the Human Otc Drug category. It is labeled and distributed by Bayer Healthcare Llc.. The primary component is Calcium Carbonate.

Product ID0280-0221_77304cd7-8ba9-64ac-e053-2991aa0ad460
NDC0280-0221
Product TypeHuman Otc Drug
Proprietary NameAlka-Seltzer Heartburn ReliefChews
Generic NameCalcium Carbonate
Dosage FormTablet, Chewable
Route of AdministrationORAL
Marketing Start Date2014-03-15
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart331
Labeler NameBayer HealthCare LLC.
Substance NameCALCIUM CARBONATE
Active Ingredient Strength750 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0280-0221-01

32 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0280-0221-01)
Marketing Start Date2020-03-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0280-0221-90 [00280022190]

Alka-Seltzer Heartburn ReliefChews TABLET, CHEWABLE
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-08-12

NDC 0280-0221-36 [00280022136]

Alka-Seltzer Heartburn ReliefChews TABLET, CHEWABLE
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2014-03-15

NDC 0280-0221-08 [00280022108]

Alka-Seltzer Heartburn ReliefChews TABLET, CHEWABLE
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-03-23

NDC 0280-0221-12 [00280022112]

Alka-Seltzer Heartburn ReliefChews TABLET, CHEWABLE
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-03-15

NDC 0280-0221-60 [00280022160]

Alka-Seltzer Heartburn ReliefChews TABLET, CHEWABLE
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2014-03-15

Drug Details

Active Ingredients

IngredientStrength
CALCIUM CARBONATE750 mg/1

OpenFDA Data

SPL SET ID:bdb43d3b-ddcd-4359-a174-a5556e7c5f57
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 308915
    • UPC Code
  • 0016500554264

    • NDC Crossover Matching brand name "Alka-Seltzer Heartburn ReliefChews" or generic name "Calcium Carbonate"

    NDCBrand NameGeneric Name
    0280-0221Alka-Seltzer Heartburn ReliefChewsAlka-Seltzer Heartburn ReliefChews
    0113-7489basic care antacidCalcium carbonate
    0113-7595basic care antacidCalcium Carbonate
    0054-3117Calcium CarbonateCalcium Carbonate
    0054-4120Calcium CarbonateCalcium Carbonate
    0054-8120Calcium CarbonateCalcium Carbonate
    0121-0766Calcium CarbonateCalcium Carbonate
    0121-4766Calcium CarbonateCalcium Carbonate
    0113-0009Good Sense Antacidcalcium carbonate
    0113-0179good sense antacidCalcium carbonate
    0113-0468good sense antacidCalcium carbonate
    0113-0478good sense antacidcalcium carbonate
    0113-0485good sense antacidcalcium carbonate
    0113-0489good sense antacidCalcium carbonate
    0113-0595good sense antacidCalcium Carbonate
    0113-0881Good Sense Antacidcalcium carbonate
    0113-0904good sense antacidCalcium carbonate
    0113-0962good sense antacidCalcium carbonate
    0135-0070TUMScalcium carbonate
    0135-0071TUMScalcium carbonate
    0135-0074TUMScalcium carbonate
    0135-0076TUMScalcium carbonate
    0135-0118TUMScalcium carbonate
    0135-0140TUMScalcium carbonate
    0135-0154TUMScalcium carbonate
    0135-0155TUMScalcium carbonate
    0135-0178TUMScalcium carbonate
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