D-CAL (CALCIUM CARBONATE) TABLET, CHEWABLE [A&Z PHARMACEUTICAL INC.]

D-CAL (CALCIUM CARBONATE) TABLET, CHEWABLE [A&Z PHARMACEUTICAL INC.]
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NDC	62211-166-60
Set ID	303bee24-d308-4b16-b382-c5f818014117
Category	HUMAN OTC DRUG LABEL
Packager	A&Z Pharmaceutical Inc.
Generic Name
Product Class
Product Number
Application Number	PART331

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Active ingredient (in each tablet)
Calcium Carbonate 750 mg

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 10 tablets for adults and 5 tablets for children in a 24 hour period.
Keep out of reach of children.
Directions
- Adults: chew 2 tablets daily.
- Children: chew 1 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, D&C red #27, flavors, magnesium stearate, sorbitol
PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

D-CAL
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62211-166
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	750 mg

Ingredient Name	Strength
Inactive Ingredients
CHOLECALCIFEROL (UNII: 1C6V77QF41)
D&C RED NO. 27 (UNII: 2LRS185U6K)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	pink	Score	no score
Shape	RECTANGLE	Size	17mm
Flavor	TROPICAL FRUIT PUNCH	Imprint Code	DCAL;AZ
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62211-166-60	60 in 1 BOTTLE; Type 0: Not a Combination Product	09/17/1997

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

Labeler - A&Z Pharmaceutical Inc. (080225262)

Registrant - A&Z Pharmaceutical Inc. (080225262)

Name	Address	ID/FEI	Business Operations
Establishment
A&Z Pharmaceutical Inc.		080225262	manufacture(62211-166)

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