D-CAL KIDS- calcium carbonate granule

D-Cal Kids by

Drug Labeling and Warnings

D-Cal Kids by is a Otc medication manufactured, distributed, or labeled by A&Z Pharmaceutical, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Calcium Carbonate 750 mg (in each pouch)

Purpose

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 1 pouch in a 24 hour period.
• use open pouch within two weeks.

Keep Out of Reach of Children

Directions

• Find the right dose on chart below based on weight, otherwise use age.
• Pour powder into cup and add 15mg (0.51 oz.) of water, stir and drink.

Dosing Chart

Weight (lbs)	Age	Dose
Under 24	Under 2 yrs	Ask a doctor
24-47	2-5 yrs	1/2 pouch
48-95	6-11 yrs	1 pouch

Inactive ingredients

Cholecalciferol, dextrose, maltodextrin, sodium citrate

Other Information

Store in a dry place.

Do not use if pouch is open or torn.

Mfg by: A&Z Pharmaceutical, Inc.

Hauppauge, NY 11788

QUESTIONS

Call toll free 1-800-480-1059 Monday through Friday 9AM-5PM

Principal Display Panel - Carton Label

D-Cal® Kids Granules

Calcium Supplement

Antacid

10 pouches

Principal Display Panel - Pouch Front Label

Principal Display Panel - Pouch Back Label

INGREDIENTS AND APPEARANCE

D-CAL KIDS 
calcium carbonate granule

Product 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)