ANTACID- calcium carbonate tablet, chewable

ANTACID by

Drug Labeling and Warnings

ANTACID by is a Otc medication manufactured, distributed, or labeled by Advance Pharmaceutical Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

(in each tablet)

Calcium Carbonate 500 mg

Purpose

Antacid

Uses

relieves

• acid indigestion
• heartburn
• sour stomach
• upset stomach associated with these symptoms

Warnings

Ask a doctor before use if you have

• kidney stones
• a calcium-restricted diet

  ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs.

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

  If pregnant or breast-feeding, ask a health professional before use.

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

Cherry flavor, dextrose, 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

Calcium Carbonate 500 mg

Antacid tablets

NDC: 17714-041-01 – 100 COUNT

INGREDIENTS AND APPEARANCE

ANTACID 
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17714-041
Route of Administration	ORAL

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

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

Product Characteristics
Color	white	Score	score with uneven pieces
Shape	ROUND	Size	16mm
Flavor	CHERRY	Imprint Code	AP;041
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17714-041-01	100 in 1 BOTTLE; Type 0: Not a Combination Product	11/30/2007

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	11/30/2007

Labeler - Advance Pharmaceutical Inc. (078301063)

Registrant - Advance Pharmaceutical Inc. (078301063)

Establishment
Name	Address	ID/FEI	Business Operations
Advance Pharmaceutical Inc.		078301063	manufacture(17714-041)