PlainRecalls
FDA Drug Low Class III Terminated

PreviDent 5000 ppm, DRY MOUTH, 1.1% Sodium Fluoride, PRESCRIPTION STRENGTH TOOTHPASTE, SLS Free Formula, SOOTHING MINT, 3.4 FL OZ (100 mL), Colgate Oral Pharmaceuticals, Inc., New York, NY 10022 --- NDC 0126-0016-61, UPC 3834110622

Reported: March 22, 2017 Initiated: February 13, 2017 #D-0521-2017

Product Description

PreviDent 5000 ppm, DRY MOUTH, 1.1% Sodium Fluoride, PRESCRIPTION STRENGTH TOOTHPASTE, SLS Free Formula, SOOTHING MINT, 3.4 FL OZ (100 mL), Colgate Oral Pharmaceuticals, Inc., New York, NY 10022 --- NDC 0126-0016-61, UPC 3834110622

Reason for Recall

Label Mix up; rear panel is incorrectly labeled with the PreviDent 5000 Enamel Protect rear panel.

Details

Recalling Firm
Colgate Palmolive Co
Units Affected
14,656 bottles
Distribution
Nationwide
Location
New York, NY

Frequently Asked Questions

What product was recalled?
PreviDent 5000 ppm, DRY MOUTH, 1.1% Sodium Fluoride, PRESCRIPTION STRENGTH TOOTHPASTE, SLS Free Formula, SOOTHING MINT, 3.4 FL OZ (100 mL), Colgate Oral Pharmaceuticals, Inc., New York, NY 10022 --- NDC 0126-0016-61, UPC 3834110622. Recalled by Colgate Palmolive Co. Units affected: 14,656 bottles.
Why was this product recalled?
Label Mix up; rear panel is incorrectly labeled with the PreviDent 5000 Enamel Protect rear panel.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 22, 2017. Severity: Low. Recall number: D-0521-2017.