PreviDent

Product NDC

0126-0179

11-digit product format

001260179

Labeler code

0126

Product ID

0126-0179_3e8f2dee-5e1c-4666-a5ac-36b1730055d2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sodium Fluoride

Dosage form

MOUTHWASH

Route

DENTAL

Labeler

Colgate Oral Pharmaceuticals, Inc.

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2012-08-29

Marketing end

0000-00-00

Substance

SODIUM FLUORIDE

Active strength

2 mg/mL

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record