Class III · Low risk
Just Right 5000
LABELING: LABEL MIX-UP.
National Drug Code
Is NDC 57511-0002-01 recalled?
Just Right 5000 · 97 g in 1 TUBE (57511-0002-1)
Yes — this exact package was recalled
1 FDA recall names the code 57511-0002-01 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
- 1.1% Sodium Fluoride Toothpaste
- Strength
- SODIUM FLUORIDE 1.1 g/100g
- Form
- Gel, Dentifrice · Topical
- Labeler
- Elevate Oral Care
- Type
- Human Prescription Drug
- Product code
- 57511-0002
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
- 57511-0611 Povi-One 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.