D-CAL KIDS- calcium carbonate tablet, chewable

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 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

INGREDIENTS AND APPEARANCE

D-CAL KIDS 
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62211-196
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

Inactive Ingredients
Ingredient Name	Strength
CHOLECALCIFEROL (UNII: 1C6V77QF41)
ASPARTAME (UNII: Z0H242BBR1)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	orange	Score	no score
Shape	FREEFORM	Size	17mm
Flavor		Imprint Code	0
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62211-196-30	30 in 1 BOTTLE; Type 0: Not a Combination Product	09/17/1997

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	09/17/1997

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(62211-196)