Label: D-CAL KIDS- calcium carbonate granule
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Contains inactivated NDC Code(s)
NDC Code(s): 62211-239-57 - Packager: A&Z Pharmaceutical, 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 October 3, 2019
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- Active ingredient
- Purpose
- Uses
- Warnings
- Keep Out of Reach of Children
- Directions
- Inactive ingredients
- Other Information
- QUESTIONS
- Principal Display Panel - Carton Label
- Principal Display Panel - Pouch Front Label
- Principal Display Panel - Pouch Back Label
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INGREDIENTS AND APPEARANCE
D-CAL KIDS
calcium carbonate granuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62211-239 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 750 mg in 1 g Inactive Ingredients Ingredient Name Strength CHOLECALCIFEROL (UNII: 1C6V77QF41) DEXTROSE (UNII: IY9XDZ35W2) MALTODEXTRIN (UNII: 7CVR7L4A2D) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62211-239-57 10 in 1 BOX 01/04/2008 1 1 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 01/04/2008 Labeler - A&Z Pharmaceutical, Inc. (080225262) Registrant - A&Z Pharmaceutical, Inc. (080225262) Establishment Name Address ID/FEI Business Operations A&Z Pharmaceutical, Inc. 080225262 manufacture(62211-239)