ULTRA STRENGTH ANTACID- calcium carbonate tablet, chewable

Ultra Strength Antacid by

Drug Labeling and Warnings

Ultra Strength Antacid by is a Otc medication manufactured, distributed, or labeled by UNITED NATURAL FOODS, INC. DBA UNFI, Guardian Drug Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT (in each tablet)

Calcium carbonate 1000 mg

PURPOSE

Antacid

USE(S)

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/BREASTFEEDING,

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

.

DIRECTIONS

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

OTHER INFORMATION

• each tablet contains: elemental calcium 400 mg, magnesium 10 mg
• do not use if printed seal under cap is torn or missing
• store at room temperature. keep the container tightly closed.

INACTIVE INGREDIENTS

corn starch, crospovidone, dextrose, flavors, magnesium stearate, maltodextrin, sucrose, talc.

PRINCIPAL DISPLAY PANEL

NDC: 83455-171-68

Compare to Tums® Ultra Strength 1000 active ingredient*

EQUALINE®

ultra strength
antacid tablets
calcium carbonate

1000 mg

Relieves

heartburn and

acid Indigestion

Peppermint flavor

72 chewable tablets

INGREDIENTS AND APPEARANCE

ULTRA STRENGTH ANTACID 
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83455-171
Route of Administration	ORAL

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

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SUCROSE (UNII: C151H8M554)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	WHITE	Score	no score
Shape	ROUND	Size	17mm
Flavor	PEPPERMINT	Imprint Code	G171
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83455-171-68	72 in 1 BOTTLE; Type 0: Not a Combination Product	02/07/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	02/07/2025

Labeler - UNITED NATURAL FOODS, INC. DBA UNFI (943556183)

Establishment
Name	Address	ID/FEI	Business Operations
Guardian Drug Company		119210276	MANUFACTURE(83455-171)