Active Ingredient

(in each tablet)

Calcium Carbonate 500 mg

Purpose

Antacid

Uses

relieves

acid indigestion
heartburn
sour stomach

Warnings

Ask a doctor before use if you have

kidney stones
a calcium-restricted diet
ask a doctor or pharmacist before use if you aretaking a prescription drug. Antacids may interact with certain prescription drugs.

Stop use and ask a doctorif symptoms last more than 2 weeks.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

chew 1-2 tablets as symptoms occurs.
do not take more than 8 tablets in 24 hours
do not use the maximum dosage for more than 2 weeks

Other Information

each tablet contains:calcium 200 mg
store at room temperature 15-30 °C (59-86 °F)

Inactive Ingredients

Al-lakes (D&C red #27, D&C yellow # 10, FD&C blue #1, FD&C yellow # 6), dextrose, flavors (cherry, lemon, lime, orange), magnesium stearate, maltodextrin

Questions or Comments

Call 631-981-4600, Monday-Friday, 8.30 am – 4.30 pm ET

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

Manufactured by: Advance Pharmaceutical Inc. Holtsville, NY 11742

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

b43c92b6-figure-01 b43c92b6-figure-02

Calcium Carbonate 500 mg

Antacid tablets

NDC: 17714-043-15 – 150 COUNT

ANTACID
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:17714-043
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	500 mg

Ingredient Name	Strength
Inactive Ingredients
DEXTROSE (UNII: IY9XDZ35W2)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CHERRY (UNII: BUC5I9595W)

Product Characteristics
Color	yellow, pink, green	Score	score with uneven pieces
Shape	ROUND	Size	16mm
Flavor	LIME (Cherry,Lemon,Orange)	Imprint Code	AP;043
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:17714-043-15	150 in 1 BOTTLE; Type 0: Not a Combination Product	01/26/1996
2	NDC:17714-043-55	55 in 1 BOTTLE; Type 0: Not a Combination Product	01/26/1996

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M001	01/26/1996

Labeler - Advance Pharmaceutical Inc. (078301063)

Registrant - Advance Pharmaceutical Inc. (078301063)

Name	Address	ID/FEI	Business Operations
Establishment
Advance Pharmaceutical Inc.		078301063	manufacture(17714-043)