Label: SUNMARK CALCIUM ANTACID- calcium carbonate tablet, chewable
- NDC Code(s): 49348-055-39
- Packager: Strategic Sourcing Services LLC
- Category: HUMAN OTC DRUG LABEL
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 6, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
- PDP
-
INGREDIENTS AND APPEARANCE
SUNMARK CALCIUM ANTACID
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49348-055 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 750 mg Inactive Ingredients Ingredient Name Strength ADIPIC ACID (UNII: 76A0JE0FKJ) ASPARTAME (UNII: Z0H242BBR1) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SORBITOL (UNII: 506T60A25R) Product Characteristics Color orange Score no score Shape ROUND Size 16mm Flavor ORANGE Imprint Code G174 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49348-055-39 80 in 1 BOTTLE; Type 0: Not a Combination Product 09/24/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 09/24/2019 Labeler - Strategic Sourcing Services LLC (116956644)