TUMS ULTRA 1000 mg/1
calcium carbonate · TABLET, CHEWABLE · Haleon US Holdings LLC
TUMS ULTRA is a tablet, chewable containing calcium carbonate at 1000 mg/1, taken oral. Manufactured by Haleon US Holdings LLC.
Key Facts
- Brand Name
- TUMS ULTRA
- Generic Name
- calcium carbonate
- NDC Code (Product)
0135-0235- Manufacturer
- Haleon US Holdings LLC
- Strength
- 1000 mg/1
- Dosage Form
- TABLET, CHEWABLE
- Route
- ORAL
- Marketing Status
- Application #
- M001
- Marketing Start
- 06/21/2021
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Frequently Asked Questions
What is TUMS ULTRA used for?
TUMS ULTRA contains calcium carbonate. It is a tablet, chewable taken oral. Consult your doctor for specific uses.
Is TUMS ULTRA a controlled substance?
TUMS ULTRA is not classified as a controlled substance by the DEA.
What is the generic name for TUMS ULTRA?
The generic name for TUMS ULTRA is calcium carbonate. There are 12 other brand versions of calcium carbonate.
What is the NDC code for TUMS ULTRA 1000 mg/1?
The NDC (National Drug Code) for TUMS ULTRA 1000 mg/1 is 0135-0235, listed by Haleon US Holdings LLC.
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- Thompson Antacid420 mg/173408-921
- Rugby Extra Strength Antacid750 mg/10536-1229
- Gas-X Total Relief Maximum Strength750 mg/10067-0119
- Meijer Wild Berry Antacid Chews750 mg/179481-0042
- equate Extra Strength Antacid750 mg/179903-102
- Equate Wild Berry Antacid Chews750 mg/179903-221
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)