Maximum Strength Sensitive

Product NDC

51009-166

11-digit product format

510090166

Labeler code

51009

Product ID

51009-166_b5fa22e2-cc30-488b-8527-87ed98a19680

Type

HUMAN OTC DRUG

Nonproprietary name

Sodium Fluoride and Potassium Nitrate

Dosage form

PASTE, DENTIFRICE

Route

DENTAL

Labeler

Tom's of Maine, Inc.

Application

part355

Marketing category

OTC MONOGRAPH FINAL

Marketing start

2009-09-01

Marketing end

0000-00-00

Substance

SODIUM FLUORIDE; POTASSIUM NITRATE

Active strength

0 g/g; g/g

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record