Class III ยท Low risk
Tums
Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted Berries 1000mg Chewable tables, may contain EX TUMS Assorted Berries 750mg tablets
National Drug Code
Is NDC 0135-0181-02 recalled?
Tums Ultra · 72 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-02)
Yes — this exact package was recalled
1 FDA recall names the code 0135-0181-02 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- calcium carbonate
- Strength
- CALCIUM CARBONATE 1000 mg/1
- Form
- Tablet, Chewable · Oral
- Labeler
- Haleon US Holdings LLC
- Type
- Human OTC Drug
- Product code
- 0135-0181
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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