Label: CALCIUM CARBONATE 500MG tablet, chewable
- NDC Code(s): 68210-5033-5
- Packager: Spirit Pharmaceuticals LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Official Label (Printer Friendly)
- DRUG FACTS
- Active Ingredient ( in each tablet) Calcium Carbonete USP 500 mg
- Purpose Antacid
- Uses relieves heartburn acid indigestion sour stomach upset stomach associated with these symptoms
- Warnings
- Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.
- When using this product
- Keep out of reach of children.
- Directions adults and children 12 years of age and over: chew 2-4 tablets as symptoms occur, or as directed by a doctordo not take for symptoms that persist for more than 2 weeks unless advised by a doctor
- Other information
- Inactive ingredients adipic acid, FD&C Blue No. 1 lake, FD&C Yellow 5 (tartrazine), FD&C Yellow 6, FD&C Red No. 40, flavors, magnesium stearate, maltodextrin, microcrystalline cellulose, sugar
- Questions or comments? 1-888-333-9792
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CALCIUM CARBONATE 500MG
calcium carbonate 500mg tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68210-5033 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 500 mg Inactive Ingredients Ingredient Name Strength ADIPIC ACID (UNII: 76A0JE0FKJ) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) FD&C RED NO. 40 (UNII: WZB9127XOA) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SUCROSE (UNII: C151H8M554) Product Characteristics Color yellow (GREEN, ORANGE, PINK) Score no score Shape ROUND Size 16mm Flavor CHERRY (ORANGE, LEMON, LIME) Imprint Code F13 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68210-5033-5 55 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/14/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 12/14/2023 Labeler - Spirit Pharmaceuticals LLC (179621011)
