QCH ULTRA STRENGTH ANTACID 171AF- calcium carbonate tablet, chewable

QCH Ultra Strength Antacid 171AF by

Drug Labeling and Warnings

QCH Ultra Strength Antacid 171AF by is a Otc medication manufactured, distributed, or labeled by Chain Drug Marketing Association Inc., 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 10mg
• do not use if printed seal under cap is torn or missing. 
• store below 30°C (86°F).

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

NDC83324-127-72

QC

QUALITY CHOICE

*Compare to the Active Ingredient in Ultra Strength Tums®

Ultra Strength
Antacid Tablets

Calcium Carbonate 1000mg

RELIEVES:

Heartburn

Acid Indigestion

Assorted Fruit

72 Chewable Tablets

INGREDIENTS AND APPEARANCE

QCH ULTRA STRENGTH ANTACID 171AF 
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83324-127
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)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SUCROSE (UNII: C151H8M554)
TALC (UNII: 7SEV7J4R1U)
CROSPOVIDONE (UNII: 2S7830E561)
ADIPIC ACID (UNII: 76A0JE0FKJ)
FD&C BLUE NO. 1 Aluminum lake (UNII: J9EQA3S2JM)
FD&C YELLOW NO. 6 ALUMINUM LAKE (UNII: GYP6Z2JR6Q)
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)

Product Characteristics
Color	PINK, ORANGE, YELLOW, GREEN	Score	no score
Shape	ROUND	Size	18mm
Flavor	CHERRY, LEMON, LIME, ORANGE	Imprint Code	G171
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83324-127-72	72 in 1 BOTTLE; Type 0: Not a Combination Product	08/03/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	08/03/2024

Labeler - Chain Drug Marketing Association Inc. (011920774)

Establishment
Name	Address	ID/FEI	Business Operations
Guardian Drug Company		119210276	MANUFACTURE(83324-127)