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    NDC 00135-0071-48 TUMS 500 mg/1 Details

    TUMS 500 mg/1

    TUMS is a ORAL TABLET 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 Information

    NDC 00135-0071
    Product ID 0135-0071_2d63d3e8-3f40-4c05-949b-e38d970f94fd
    Associated GPIs 48300010000510
    GCN Sequence Number 002689
    GCN Sequence Number Description calcium carbonate TAB CHEW 200(500)MG ORAL
    HIC3 D4B
    HIC3 Description ANTACIDS
    GCN 07893
    HICL Sequence Number 001163
    HICL Sequence Number Description CALCIUM CARBONATE
    Brand/Generic Brand
    Proprietary Name TUMS
    Proprietary Name Suffix n/a
    Non-Proprietary Name calcium carbonate
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name CALCIUM CARBONATE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part331
    Listing Certified Through 2024-12-31

    Package

    NDC 00135-0071-48 (00135007148)

    NDC Package Code 0135-0071-48
    Billing NDC 00135007148
    Package 12 TABLET in 1 PACKAGE (0135-0071-48)
    Marketing Start Date 2010-03-10
    NDC Exclude Flag N
    Pricing Information N/A
    << 00135-0071-27 00135-0074-01 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL 35f79dcf-1743-4d9f-aba5-5ead6b056309 Details

    Revised: 12/2020
    Document Id: 2d63d3e8-3f40-4c05-949b-e38d970f94fd
    Set id: 35f79dcf-1743-4d9f-aba5-5ead6b056309
    Version: 10
    Effective Time: 20201201