Label: TUMS- calcium carbonate tablet
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NDC Code(s):
0135-0070-03,
0135-0070-27,
0135-0070-48,
0135-0071-27, view more0135-0071-48
- Packager: GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 1, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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
taking a prescription drug. Antacids may interact with certain prescription drugs.
- Directions
- Other information
- Inactive ingredients (assorted fruit)
- Inactive ingredient (peppermint)
- Questions?
- PRINCIPAL DISPLAY PANEL
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
TUMS
calcium carbonate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-0071 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 500 mg Inactive Ingredients Ingredient Name Strength ADIPIC ACID (UNII: 76A0JE0FKJ) STARCH, CORN (UNII: O8232NY3SJ) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) MINERAL OIL (UNII: T5L8T28FGP) SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L) SUCROSE (UNII: C151H8M554) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color PINK (orange, yellow, green) Score no score Shape ROUND Size 16mm Flavor CHERRY (assorted fruit, orange, lemon, lime) Imprint Code TUMS Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0135-0071-27 150 in 1 BOTTLE; Type 0: Not a Combination Product 03/10/2010 2 NDC:0135-0071-48 12 in 1 PACKAGE; Type 0: Not a Combination Product 03/10/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 03/10/2010 TUMS
calcium carbonate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-0070 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 500 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) MINERAL OIL (UNII: T5L8T28FGP) SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L) SUCROSE (UNII: C151H8M554) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color WHITE Score no score Shape ROUND Size 16mm Flavor PEPPERMINT Imprint Code TUMS Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0135-0070-03 3 in 1 CELLO PACK 03/10/2010 1 12 in 1 PACKAGE; Type 0: Not a Combination Product 2 NDC:0135-0070-27 150 in 1 BOTTLE; Type 0: Not a Combination Product 03/10/2010 3 NDC:0135-0070-48 12 in 1 PACKAGE; Type 0: Not a Combination Product 03/10/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 03/10/2010 Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)