Maximum Strength Sensitive

Product NDC

51009-167

11-digit product format

510090167

Labeler code

51009

Product ID

51009-167_3195bbb3-68cd-430a-ab3d-9d0e6332631a

Type

HUMAN OTC DRUG

Nonproprietary name

Sodium Fluoride and Potassium Nitrate

Dosage form

PASTE, DENTIFRICE

Route

DENTAL

Labeler

Tom's of Maine, Inc.

Application

part356

Marketing category

OTC MONOGRAPH NOT 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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record