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FDAFDA · Food and drugs·Recall number D-0521-2017

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

Published March 22, 2017 · Recall initiated: February 13, 2017

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
PREVIDENT
Manufacturer
Colgate Palmolive Co
Distributor
Nationwide
UPC
0301260016610
Lot
Lots: 6350US561G, 6350US562G, 6351US561G, 6351US562G
Risk classification
Class III
Area (FDA)
drug
Country
United States

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