NDC 0135-0180

TUMS ULTRA

Calcium Carbonate

TUMS ULTRA is a Oral Tablet, Chewable in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Calcium Carbonate.

Product ID0135-0180_1331eab0-b64d-4db5-a091-93bdd99f9ade
NDC0135-0180
Product TypeHuman Otc Drug
Proprietary NameTUMS ULTRA
Generic NameCalcium Carbonate
Dosage FormTablet, Chewable
Route of AdministrationORAL
Marketing Start Date2010-02-12
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart331
Labeler NameGlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Substance NameCALCIUM CARBONATE
Active Ingredient Strength1000 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0135-0180-01

86 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-01)
Marketing Start Date2010-02-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0135-0180-05 [00135018005]

TUMS ULTRA TABLET, CHEWABLE
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-12
Marketing End Date2014-01-21

NDC 0135-0180-01 [00135018001]

TUMS ULTRA TABLET, CHEWABLE
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-12
Inactivation Date2020-01-31

NDC 0135-0180-07 [00135018007]

TUMS ULTRA TABLET, CHEWABLE
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-12
Marketing End Date2014-01-21

NDC 0135-0180-04 [00135018004]

TUMS ULTRA TABLET, CHEWABLE
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-12
Marketing End Date2014-01-21

NDC 0135-0180-14 [00135018014]

TUMS ULTRA TABLET, CHEWABLE
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2010-02-12
Inactivation Date2020-01-31

NDC 0135-0180-02 [00135018002]

TUMS ULTRA TABLET, CHEWABLE
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2010-02-12
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CALCIUM CARBONATE1000 mg/1

OpenFDA Data

SPL SET ID:f4786707-a0f7-4ba8-9656-06278d1b4b6c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1044524
  • 308892

    • NDC Crossover Matching brand name "TUMS ULTRA" or generic name "Calcium Carbonate"

    NDCBrand NameGeneric Name
    0135-0228TUMS ULTRATUMS ULTRA
    0135-0180TUMS ULTRATUMS ULTRA
    0135-0181TUMS ULTRATUMS ULTRA
    0135-0540TUMS ULTRATUMS ULTRA
    0135-0610TUMS ULTRATUMS ULTRA
    0135-0612TUMS ULTRATUMS ULTRA
    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

    Trademark Results [TUMS]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    TUMS
    TUMS
    98794008 not registered Live/Pending
    Haleon US IP LLC
    2024-10-10
    TUMS
    TUMS
    98058821 not registered Live/Pending
    BANG, Hai Hwa
    2023-06-26
    TUMS
    TUMS
    79373831 not registered Live/Pending
    BANG, Hai Hwa
    2023-05-30
    TUMS
    TUMS
    78226130 not registered Dead/Abandoned
    SmithKline Beecham Corporation
    2003-03-17
    TUMS
    TUMS
    77619345 3741016 Live/Registered
    GLAXOSMITHKLINE CONSUMER HEALTHCARE (US) IP LLC
    2008-11-21
    TUMS
    TUMS
    77155155 not registered Dead/Abandoned
    GLAXOSMITHKLINE LLC
    2007-04-12
    TUMS
    TUMS
    75696786 not registered Dead/Abandoned
    SmithKline Beecham Corporation
    1999-05-03
    TUMS
    TUMS
    75676521 2441507 Dead/Cancelled
    GLAXOSMITHKLINE LLC
    1999-04-07
    TUMS
    TUMS
    75465207 2240777 Dead/Cancelled
    SmithKline Beecham Corporation
    1998-04-09
    TUMS
    TUMS
    75058334 2076469 Live/Registered
    GLAXOSMITHKLINE CONSUMER HEALTHCARE (US)
    1996-02-15
    TUMS
    TUMS
    74723028 1979916 Live/Registered
    GLAXOSMITHKLINE CONSUMER HEALTHCARE (US) IP LLC
    1995-08-30
    TUMS
    TUMS
    74722865 1979915 Live/Registered
    GLAXOSMITHKLINE CONSUMER HEALTHCARE (US) IP LLC
    1995-08-30
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.