QUALITY CHOICE REGULAR STRENGTH ANTACID 126 REGULAR STRENGTH ANTACID- calcium carbonate tablet, chewable

Quality Choice Regular Strength Antacid 126 by

Drug Labeling and Warnings

Quality Choice Regular Strength Antacid 126 by is a Otc medication manufactured, distributed, or labeled by Chain Drug Marketing Association Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT (in each tablet)

Calcium carbonate 500 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 15 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 2-4 tablets as symptoms occur, or as directed by a doctor.

OTHER INFORMATION

• each tablet contains: elemental calcium 200 mg
• do not use if printed seal under cap is torn or missing. 
• store below 30ºC(86ºF). 

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

NDC: 83324-123-15

QUALITY CHOICE

*Compare to the Active ingredient in Regular Strength Tums®

Regular Strength

Antacid TabletsCalcium Carbonate 500 mg

Relieves:

Heartburn

Acid Indigestion

Assorted Fruit 
150 Chewable Tablets

INGREDIENTS AND APPEARANCE

QUALITY CHOICE REGULAR STRENGTH ANTACID 126  REGULAR STRENGTH ANTACID
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83324-123
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
ADIPIC ACID (UNII: 76A0JE0FKJ)
STARCH, CORN (UNII: O8232NY3SJ)
CROSPOVIDONE (UNII: 2S7830E561)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SUCROSE (UNII: C151H8M554)
TALC (UNII: 7SEV7J4R1U)
D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)
D&C RED NO. 30 ALUMINUM LAKE (UNII: GE75M6YV5W)
D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6)
FD&C YELLOW NO. 6 ALUMINUM LAKE (UNII: GYP6Z2JR6Q)

Product Characteristics
Color	ORANGE, YELLOW, GREEN, PINK (reddish pink)	Score	no score
Shape	ROUND	Size	16mm
Flavor	CHERRY, LEMON, LIME, ORANGE	Imprint Code	G126
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83324-123-15	150 in 1 BOTTLE; Type 0: Not a Combination Product	06/28/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	06/28/2024

Labeler - Chain Drug Marketing Association Inc. (011920774)