Search by Drug Name or NDC

NDC 17714-0041-01 ANTACID 500 mg/1 Details

ANTACID 500 mg/1

ANTACID is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Advance Pharmaceutical Inc.. The primary component is CALCIUM CARBONATE.

MedlinePlus Drug Summary

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 17714-0041-01
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	17714-0041
Product ID	17714-041_999a325a-9e12-4c31-e053-2a95a90a4f1e
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	ANTACID
Proprietary Name Suffix	n/a
Non-Proprietary Name	Calcium Carbonate
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	CALCIUM CARBONATE
Labeler Name	Advance Pharmaceutical Inc.
Pharmaceutical Class	Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part331
Listing Certified Through	2024-12-31

Package

Package Images

NDC 17714-0041-01 (17714004101)

Pricing Information	N/A
NDC Package Code	17714-041-01
Billing NDC	17714004101
Package	100 TABLET, CHEWABLE in 1 BOTTLE (17714-041-01)
Marketing Start Date	2007-11-30
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 3203dfc5-2cb1-4703-8d81-63fba07ddd98 Details

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

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

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

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

Labeler - Advance Pharmaceutical Inc. (078301063)

Registrant - Advance Pharmaceutical Inc. (078301063)

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

Revised: 12/2019

Document Id: 999a325a-9e12-4c31-e053-2a95a90a4f1e

Set id: 3203dfc5-2cb1-4703-8d81-63fba07ddd98

Version: 2

Effective Time: 20191213