Denti-Care Denti-Pro

Product NDC

64778-0218

11-digit product format

647780218

Labeler code

64778

Product ID

64778-0218_7e41878e-b946-5a65-e053-2a91aa0ab3e3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sodium Fluoride

Dosage form

GEL

Route

DENTAL

Labeler

AMD Medicom Inc.

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2005-04-01

Marketing end

2020-12-31

Substance

SODIUM FLUORIDE

Active strength

0 g/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record