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Ultra Strength

Dosage form
TABLET, CHEWABLE
Labeler
BETTER LIVING BRANDS LLC
Label updated
2025-10-29
Retrieved
2026-09-07
Active ingredients
CALCIUM CARBONATE
View original label and images on DailyMed ↗
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 presentlytaking 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.
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

[Image in the official label — see DailyMed source]

Package Label 72 Chewable Tablets

[Image in the official label — see DailyMed source]

DailyMed Set ID: 35b3d9d0-b04d-4f6d-b99d-435233803d4b · Version 6
NDC: 21130-310