Label: ANTACID RELIEF- calcium carbonate tablet, chewable
- NDC Code(s): 21130-472-68
- Packager: Safeway
- 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 January 22, 2016
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- Active ingredient (in each tablet)
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- Inactive ingredients
- PDP
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INGREDIENTS AND APPEARANCE
ANTACID RELIEF
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-472 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 1000 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) CROSPOVIDONE (UNII: 68401960MK) DEXTROSE (UNII: IY9XDZ35W2) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) SUCROSE (UNII: C151H8M554) TALC (UNII: 7SEV7J4R1U) 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:21130-472-68 72 in 1 BOTTLE; Type 0: Not a Combination Product 11/11/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 11/11/2015 Labeler - Safeway (009137209) Establishment Name Address ID/FEI Business Operations Guardian Drug Company 119210276 manufacture(21130-472)