Label: TUMS EXTRA STRENGTH, SMOOTHIES- calcium carbonate tablet, chewable
- NDC Code(s): 0135-1002-01
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 14, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient (per tablet)
- Purpose
- Uses
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Warnings
Ask a doctor or pharmacist before use if you are
presently taking a prescription drug. Antacids may interact with certain prescription drugs.
- Directions
- Other information
- Inactive ingredients
- Questions?
- Additional information
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
TUMS EXTRA STRENGTH, SMOOTHIES
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-1002 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE 750 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SORBITOL (UNII: 506T60A25R) SUCROSE (UNII: C151H8M554) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color WHITE Score no score Shape ROUND Size 19mm Flavor PEPPERMINT Imprint Code TUMS;SD Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0135-1002-01 140 in 1 BOTTLE; Type 0: Not a Combination Product 11/29/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 11/29/2021 Labeler - Haleon US Holdings LLC (079944263)

