UP AND UP EXTRA STRENGTH ANTACID 173 BERRY FUSION- calcium carbonate tablet, chewable

up and up Extra Strength Antacid 173 Berry Fusion by

Drug Labeling and Warnings

up and up Extra Strength Antacid 173 Berry Fusion by is a Otc medication manufactured, distributed, or labeled by Target corporation, Guardian Drug Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT (in each tablet)

Calcium carbonate 750 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 10 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:
• 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 300 mg, magnesium 10mg
• store at room temperature. keep the container tightly closed.

INACTIVE INGREDIENTS

adipic acid, corn starch, dextrose, FD&C blue 1 lake, FD&C red 40 lake, flavors, magnesium stearate, maltodextrin, microcrystalline cellulose, sorbitol, sucrose, talc.

PRINCIPAL DISPLAY PANEL

NDC: 82242-010-23

Compare to active ingredient in TUMS® SmoothiesTM E-X*

Extra Strength

Antacid 

Calcium Carbonate, 750 mg
Smooth dissolving

 Provides fast relief from heartburn, acid indigestion and upset stomach

Berry Fusion Flavors

up&up

60 Tablets
60 CHEWABLE TABLETS

   

INGREDIENTS AND APPEARANCE

UP AND UP EXTRA STRENGTH ANTACID 173 BERRY FUSION 
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82442-010
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	750 mg

Inactive Ingredients
Ingredient Name	Strength
ADIPIC ACID (UNII: 76A0JE0FKJ)
STARCH, CORN (UNII: O8232NY3SJ)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)
FD&C RED NO. 40 ALUMINUM LAKE (UNII: 6T47AS764T)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SUCROSE (UNII: C151H8M554)
TALC (UNII: 7SEV7J4R1U)
SORBITOL (UNII: 506T60A25R)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)

Product Characteristics
Color	PINK (light pink) , RED (light red) , ORANGE (light orange) , YELLOW (light yellow)	Score	no score
Shape	ROUND	Size	18mm
Flavor	CHERRY, LEMON, ORANGE, STRAWBERRY	Imprint Code	G173
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82442-010-23	60 in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	part331	06/17/2024

Labeler - Target corporation (006961700)

Establishment
Name	Address	ID/FEI	Business Operations
Guardian Drug Company		119210276	MANUFACTURE(82442-010)