Label: TOPCARE ULTRA STRENGTH ANTACID PEPPERMINT- calcium carbonate tablet, chewable
- NDC Code(s): 76162-131-68
- Packager: Topco Associates, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT (in each tablet)
- PURPOSE
- USE(S)
- WARNINGS
- ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE
- WHEN USING THIS PRODUCT
- IF PREGNANT OR/BREASTFEEDING,
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
TOPCARE ULTRA STRENGTH ANTACID PEPPERMINT
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76162-131 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 1000 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) SUCROSE (UNII: C151H8M554) TALC (UNII: 7SEV7J4R1U) CROSPOVIDONE (UNII: 2S7830E561) Product Characteristics Color WHITE Score no score Shape ROUND Size 17mm Flavor PEPPERMINT Imprint Code G171 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76162-131-68 72 in 1 BOTTLE; Type 0: Not a Combination Product 04/25/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 04/25/2022 Labeler - Topco Associates, LLC (006935977)