QUALITY CHOICE Ultra Strength
- Dosage form
- TABLET, CHEWABLE
- Labeler
- QUALITY CHOICE (Chain drug Marketing Assoiciation)
- Label updated
- 2025-12-04
- Retrieved
- 2026-09-07
- Active ingredients
- CALCIUM CARBONATE
Active ingredient (per tablet)
Calcium Carbonate USP 1000mg
Purpose
Antacid
Uses
relieves
- heartburn
- acid indigestion
- sour stomach
- upset stomach associated with these symptoms
Ask a doctor or pharmacist before use if you are
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.
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 room temperature.Keep the container tightly closed
Safety sealed: Do not use if printed seal under cap is torn or missing.
Inactive ingredients
adipic acid, dextrose, FD&C Blue No.1 lake, Red No.40 lake, flavors, magnesium stearate, maltodextrin, starch, sucralose.
Questions or comments?
1-866-467-2748
Package/Label Principal Display Panel
* Compare to the active ingredient in Ultra Strength Tums®
QUALITY CHOICE ®
NDC# 83324-317-72
Ultra Strength
Antacid Tablets
Calcium Carbonate 1000 mg
Relieves:
- Upset Stomach
- Heartburn
- Acid Indigestion
Assorted Berry
Naturally and Artificially Flavored
GLUTEN FREE
72 CHEWABLE TABLETS
K PAREVE
QC SATISFACTION GURANTEED
Distributed by: C.D.M.A., Inc.
Novi, MI 48376-0995
www.qualitychoice.com
Questions: 800-935-2362
*This product is not manufactured or distributed by GlaxoSmithKline, the owner of the registered trademark, Ultra Strength Tums ®.
[Image in the official label — see DailyMed source]
DailyMed Set ID: b074a885-5d10-46e4-8de9-dd9460968dad · Version 2
NDC: 83324-317