UP AND UP ULTRA STRENGTH ANTACID 1000- calcium carbonate tablet, chewable

up and up ultra strength antacid 1000 by

Drug Labeling and Warnings

up and up ultra strength antacid 1000 by is a Otc medication manufactured, distributed, or labeled by Target Corporation, VIRCHOW BIOTECH PRIVATE LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient (per tablet)

Calcium Carbonate USP 1000mg

Purpose

Antacid

Uses

relieves heartburn acid indigestion sour stomach upset stomach associated with these symptoms

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 24 hours
if pregnant do not take more than 5 tablets in 24 hours
do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor

Keep out of reach of children.

Directions

adults and children 12 years of age and over: chew 2-3 tablets completely as symptoms occur, or as directed by a doctor. Do not swallow tablets whole.
do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Other information

each tablet contains: calcium 400mg
store at controlled room temperature. Keep the container tightly closed.

Inactive ingredients

adipic acid, D&C Yellow No.10 Lake, dextrose, FD&C Red No. 40 Lake, FD&C Yellow No. 6 Lake, flavors, magnesium stearate, maltodextrin, starch, sucralose.

Questions or comments?

call 1-800-910-6874

SPL UNCLASSIFIED SECTION

Compare to active ingredient in Tums Ultra®*

TROPICAL FRUIT FLAVOR

naturally and artificially flavored

DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING.

Distributed by
Target Corp.
Mpls., MN 55403
Made in India
TM & ©2023 Target Brands, Inc.

*This product is not manufactured or distributed by GlaxoSmithKline LLC, owner of the registered trademark, Ultra Strength TUMS®.

Packaging

INGREDIENTS AND APPEARANCE

UP AND UP ULTRA STRENGTH ANTACID 1000 
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82442-101
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
ADIPIC ACID (UNII: 76A0JE0FKJ)
D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
STARCH, CORN (UNII: O8232NY3SJ)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Characteristics
Color	white, yellow, orange, pink	Score	no score
Shape	ROUND	Size	19mm
Flavor	FRUIT (TROPICAL FRUIT FLAVOR)	Imprint Code	VB101
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82442-101-72	72 in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	04/07/2023

Labeler - Target Corporation (006961700)

Registrant - VIRCHOW BIOTECH PRIVATE LIMITED (737786315)

Establishment
Name	Address	ID/FEI	Business Operations
VIRCHOW BIOTECH PRIVATE LIMITED		737786315	manufacture(82442-101)