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D-Cal Kids by A&Z Pharmaceutical, Inc.

Dosage form: tablet, chewable
Ingredients: CALCIUM CARBONATE 750mg
Labeler: A&Z Pharmaceutical, Inc.
NDC Code: 62211-196

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.

D-Cal Kids

ACTIVE INGREDIENTS

Calcium Carbonate 750 mg

PURPOSES

Antacid

USES

Relieves

  • heartburn
  • acid indigestion
  • sour stomach
  • upset stomach due to these symptoms

WARNINGS

Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs. When using this product do not take more than 5 tablets in a 24 hour period. Keep out of reach of children.

Keep out of reach of children

Directions
  • chew one tablet daily. If symptoms persist, ask a doctor.

Other Information
  • store in a dry place
  • do not use if imprinted seal under cap is torn or open

Inactive ingredients

cholecalciferol, aspartame, citric acid, D&C Yellow #6, FD&C Blue #1, FD&C Red #40, FD&C Yellow #5, FD&C Yellow #10, flavors, magnesium stearate, sorbitol

PRINCIPAL DISPLAY PANEL

D-CAL KIDS 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62211-196
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (CALCIUM CATION and CARBONATE ION) CALCIUM CARBONATE750 mg
Inactive Ingredients
Ingredient NameStrength
CHOLECALCIFEROL 
ASPARTAME 
CITRIC ACID MONOHYDRATE 
FD&C BLUE NO. 1 
FD&C RED NO. 40 
FD&C YELLOW NO. 5 
FD&C YELLOW NO. 6 
D&C YELLOW NO. 10 
MAGNESIUM STEARATE 
SORBITOL 
Product Characteristics
ColororangeScoreno score
ShapeFREEFORMSize17mm
FlavorImprint Code0
Contains    
Packaging
#Item CodePackage Description
1NDC:62211-196-3030 TABLET, CHEWABLE (TABLET) in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33109/17/1997
Labeler - A&Z Pharmaceutical, Inc. (926820705)
Registrant - A&Z Pharmaceutical, Inc. (964848795)
Establishment
NameAddressID/FEIOperations
A&Z Pharmaceutical, Inc.964848795manufacture(62211-196)

Revised: 12/2013
 
A&Z Pharmaceutical, Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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