Class III ยท Low risk
3M ESPE Clinpro 5000
Labeling: Incorrect or Missing Lot and/or Exp. Date - The subject lot is missing the lot number and expiration date stamp on the primary box..
National Drug Code
Is NDC 48878-3130-04 recalled?
Clinpro 5000 · 1 TUBE in 1 BOX (48878-3130-4) / 113 g in 1 TUBE
Yes — this exact package was recalled
1 FDA recall names the code 48878-3130-04 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
- sodium fluoride
- Strength
- SODIUM FLUORIDE 5 mg/g
- Form
- Paste, Dentifrice · Oral
- Labeler
- Solventum US LLC
- Type
- Human Prescription Drug
- Product code
- 48878-3130
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.
Free recall alerts
Know the day your medication is recalled
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