Denti-Care Denti-Pro

Product NDC

64778-0213

11-digit product format

647780213

Labeler code

64778

Product ID

64778-0213_7e1f6086-dccd-4384-e053-2991aa0abe7d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sodium Fluoride

Dosage form

GEL

Route

DENTAL

Labeler

AMD Medicom Inc.

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

1999-12-01

Marketing end

0000-00-00

Substance

SODIUM FLUORIDE

Active strength

0 g/mL

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record