ULTRA STRENGTH- calcium carbonate tablet, chewable

Ultra Strength by

Drug Labeling and Warnings

Ultra Strength by is a Otc medication manufactured, distributed, or labeled by BETTER LIVING BRANDS LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (per tablet)

Calcium Carbonate USP 1,000mg

Purpose

Antacid

Uses

relieves

• heartburn
• sour stomach
• acid indigestion
• 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 as symptoms occur, or as directed by a doctor
• do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Other information

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

Inactive ingredients

adipic acid, D&C Red No. 27 Lake, D&C Yellow No.10 Lake, dextrose, FD&C Blue No. 1 Lake, FD&C Yellow No. 6, flavor, magnesium stearate, maltodextrin, starch, sucralose.

Questions or comments?

1-866-467-2748

SAFETY SEALED: DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING

Package/Label Principal Display Panel

*Compare to the active ingredients in Ultra Strength Tums®

ULTRA STRENGTH

Antacid Tablets

Calcium Carbonate 1000mg

Relieves of:

• Acid indigestion
• Sour Stomach
• Heartburn

Assorted Fruit Flavors

GLUTEN-FREE

Distributed by:

*This product is not manufactured and distributed by GlaxoSmithKline LLC, owner of the registered trademark, Ultra Strength Tums®

Package Label 160 Chewable Tablets

Package Label 72 Chewable Tablets

INGREDIENTS AND APPEARANCE

ULTRA STRENGTH 
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21130-310
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	1000 mg

Inactive Ingredients
Ingredient Name	Strength
ADIPIC ACID (UNII: 76A0JE0FKJ)
D&C RED NO. 27 (UNII: 2LRS185U6K)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
STARCH, CORN (UNII: O8232NY3SJ)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Characteristics
Color	RED, YELLOW, ORANGE, GREEN	Score	no score
Shape	ROUND	Size	19mm
Flavor	FRUIT (Assorted)	Imprint Code	RP103
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21130-310-60	160 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/30/2020
2	NDC: 21130-310-72	72 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	09/30/2020

Labeler - BETTER LIVING BRANDS LLC (009137209)