- Active ingredient (in each tablet)
- Purpose
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Warnings
- Directions
- Inactive ingredients
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
ULTRA STRENGTH ANTACID RELIEF ASSORTED FRUIT
calcium antacid tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-171 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 1000 mg Inactive Ingredients Ingredient Name Strength ADIPIC ACID (UNII: 76A0JE0FKJ) STARCH, CORN (UNII: O8232NY3SJ) CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561) D&C RED NO. 27 (UNII: 2LRS185U6K) D&C RED NO. 30 (UNII: 2S42T2808B) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) SUCROSE (UNII: C151H8M554) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color orange, yellow, green, pink (reddish-pink) Score no score Shape ROUND Size 17mm Flavor FRUIT (orange, cherry, lemon, lime) Imprint Code G171 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21130-171-68 72 in 1 BOTTLE; Type 0: Not a Combination Product 08/08/2015 2 NDC:21130-171-75 160 in 1 BOTTLE; Type 0: Not a Combination Product 08/08/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 08/08/2015 Labeler - Safeway (009137209)