Label: ANTACID- calcium carbonate tablet
- NDC Code(s): 69396-142-01, 69396-142-05
- Packager: Trifecta Pharmaceuticals USA LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 27, 2024
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- Official Label (Printer Friendly)
- Active Ingredient (in each tablet)
- Purpose
- Uses
- Directions
- Warnings
- Ask a doctor or pharmacist before use if you
- Keep out of reach of children
- Other Information
- Inactive Ingredients
- Questions or Comments?
- When using this product
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INGREDIENTS AND APPEARANCE
ANTACID
calcium carbonate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69396-142 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 420 mg Inactive Ingredients Ingredient Name Strength ASPARTAME (UNII: Z0H242BBR1) MAGNESIUM STEARATE (UNII: 70097M6I30) SORBITOL (UNII: 506T60A25R) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) MALTODEXTRIN (UNII: 7CVR7L4A2D) MINT (UNII: FV98Z8GITP) Product Characteristics Color white Score score with uneven pieces Shape ROUND Size 11mm Flavor MINT Imprint Code AZ036 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69396-142-01 50 in 1 BOX 08/08/2023 1 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:69396-142-05 10000 in 1 BAG 08/08/2023 2 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 08/08/2023 Labeler - Trifecta Pharmaceuticals USA LLC (079424163)