OTC Medication Information: D-Cal Kids

D-CAL KIDS- calcium carbonate granule
A&Z Pharmaceutical, Inc.

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.

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

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

Principal Display Panel — Carton Label

Carton
(click image for full-size original)

D-CalĀ® Kids Granules

Calcium Supplement

Antacid

10 pouches

Principal Display Panel — Pouch Front Label

pouch front
(click image for full-size original)

Principal Display Panel — Pouch Back Label

Pouch back
(click image for full-size original)
D-CAL KIDS
calcium carbonate granule
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62211-239
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CALCIUM CARBONATE (CALCIUM CATION and CARBONATE ION) CALCIUM CARBONATE 750 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
CHOLECALCIFEROL
DEXTROSE
MALTODEXTRIN
SODIUM CITRATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62211-239-57 10 POUCH in 1 BOX contains a POUCH
1 1 g in 1 POUCH This package is contained within the BOX (62211-239-57)
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 Operations
A&Z Pharmaceutical, Inc. 080225262 manufacture (62211-239)

Revised: 10/2019 A&Z Pharmaceutical, Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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