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NDC 69842-0171-72 Ultra Strength Antacid 1000 mg/1 Details

Ultra Strength Antacid 1000 mg/1

Ultra Strength Antacid is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by CVS. 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: 69842-0171-72
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	69842-0171
Product ID	69842-171_ce8cfb77-e2d9-42a6-985c-534591993edb
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	Ultra Strength Antacid
Proprietary Name Suffix	n/a
Non-Proprietary Name	Calcium Antacid
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	1000
Active Ingredient Units	mg/1
Substance Name	CALCIUM CARBONATE
Labeler Name	CVS
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 69842-0171-72 (69842017172)

Pricing Information	N/A
NDC Package Code	69842-171-72
Billing NDC	69842017172
Package	160 TABLET, CHEWABLE in 1 BOTTLE (69842-171-72)
Marketing Start Date	2011-12-09
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 51acc196-ab1f-49ea-8a59-f06309f1953b Details

Active ingredient (in each tablet)

Calcium carbonate 1000 mg

Purpose

Antacid

SPL UNCLASSIFIED SECTION

Uses

relieves

acid indigestion
heartburn

Warnings

Ask a doctor or pharmacist before use if you are

presently taking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

do not take more than 7 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

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

Keep out of reach of children.

Directions

adults and children 12 years of age and over: chew 2-3 tablets as symptoms occur, or as directed by a doctor.

Other information

each tablet contains: elemental calcium 400 mg
do not use if printed seal under cap is torn or missing.
store at room temperature. keep the container tightly closed.

Inactive ingredients

adipic acid, corn starch, crospovidone, D&C red 27 lake, D&C red 30 lake, D&C yellow 10 lake, dextrose, FD&C blue 1 lake, FD&C yellow 6 lake, flavors, magnesium stearate, maltodextrin, sucrose, talc.

Principal Display Panel

CVS Health

Compare to active ingredient in TUMS® Ultra strength

Ultra Strength Antacid Tablets

Calcium Carbonate 1000 mg

Assorted Fruit Flavor

72 Chewable Tablets

INGREDIENTS AND APPEARANCE

ULTRA STRENGTH ANTACID

calcium antacid tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69842-171
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CATION	1000 mg

Ingredient Name	Strength
Inactive Ingredients
ADIPIC ACID (UNII: 76A0JE0FKJ)
STARCH, CORN (UNII: O8232NY3SJ)
CROSPOVIDONE (UNII: 2S7830E561)
D&C RED NO. 27 (UNII: 2LRS185U6K)
D&C RED NO. 30 (UNII: 2S42T2808B)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
DEXTROSE (UNII: IY9XDZ35W2)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SUCROSE (UNII: C151H8M554)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	orange, yellow, green, pink (reddish-pink)	Score	no score
Shape	ROUND	Size	17mm
Flavor	FRUIT (orange, cherry, lemon, lime)	Imprint Code	G171
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:69842-171-68	72 in 1 BOTTLE; Type 0: Not a Combination Product	12/09/2011
2	NDC:69842-171-72	160 in 1 BOTTLE; Type 0: Not a Combination Product	12/09/2011

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	12/09/2011

Labeler - CVS (062312574)

Revised: 8/2017

Document Id: ce8cfb77-e2d9-42a6-985c-534591993edb

Set id: 51acc196-ab1f-49ea-8a59-f06309f1953b

Version: 1

Effective Time: 20170809