Label: ANTACID- calcium carbonate tablet
- NDC Code(s): 17714-025-01, 17714-025-10
- Packager: Advance Pharmaceutical Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 22, 2017
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- Active Ingredient
- Purpose
- Uses
- Warnings
- Keep out of reach of children.
- Directions
- Other Information
- Inactive Ingredients
- Questions or Comments
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTACID
calcium carbonate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17714-025 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 648 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white (off) Score no score Shape ROUND Size 11mm Flavor Imprint Code AP;025 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17714-025-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 04/06/1990 2 NDC:17714-025-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 04/06/1990 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 04/06/1990 Labeler - Advance Pharmaceutical Inc. (078301063) Registrant - Advance Pharmaceutical Inc. (078301063) Establishment Name Address ID/FEI Business Operations Advance Pharmaceutical Inc. 078301063 manufacture(17714-025)