Colgate Palmolive Co recalls PreviDent 5000 ppm, DRY MOUTH, 1.1% Sodium Fluoride, PRESCRIPTION STRENGTH TOOTHPASTE, SLS Free Formula, SOOTHING MINT,…

Recall date

February 13, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0521-2017

FDA classification

Class III

Brand / firm

Colgate Palmolive Co

Sold / distributed

Nationwide

Why it was recalled

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

Class III means the product violates regulations but is not likely to cause harm.

What 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