Label: MAGNACAL- calcium carbonate tablet, chewable
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Contains inactivated NDC Code(s)
NDC Code(s): 51532-0303-2 - Packager: Afassco Inc.
- 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 September 21, 2019
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- OTHER SAFETY INFORMATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MAGNACAL
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51532-0303 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE 420 Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) SUCROSE (UNII: C151H8M554) MAGNESIUM STEARATE (UNII: 70097M6I30) MINT (UNII: FV98Z8GITP) ACACIA (UNII: 5C5403N26O) MALTODEXTRIN (UNII: 7CVR7L4A2D) Product Characteristics Color white (WHITE) Score no score Shape ROUND Size 12mm Flavor MINT Imprint Code FR8 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51532-0303-2 2 in 1 PACKET; Type 0: Not a Combination Product 10/25/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 04/07/2015 Labeler - Afassco Inc. (609982723) Registrant - ULTRAtab Laboratories, Inc. (151051757) Establishment Name Address ID/FEI Business Operations ULTRA SEAL CORPORATION 085752004 pack(51532-0303) Establishment Name Address ID/FEI Business Operations ULTRATAB LABORATORIES, INC. 151051757 manufacture(51532-0303)