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DentiCare Denti-Pro

Package insert / prescribing information
Generic name: sodium fluoride
Dosage form: gel
Drug class: Mouth and throat products

Medically reviewed by Last updated on Nov 22, 2021.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

General Information

AMD Medicom Inc.

DentiCare Pro-Gel

2% Neutral Sodium Fluoride Gel

Topical Fluoride Applications (0.9% Fluoride Ions)


16.23 fl oz / 480mL

NDC 64778-0236-1

NPN 80008850

Item Code 10023-M

Indications and Directions

Indications: Topical anti-carie preparation in a pH 7 thixotropic gel base.


Following prophylaxis treatment, fll 1/3 of tray with gel

Insert tray in the patient’s mouth,
Have patient bite down lightly for 4 minutes

Remove tray and have patient expectorate excess.

Advise patient not to eat, drink or rinse for 30 minutes after application

Medicinal ingredients: Fluoride ions 0.9% w/w (from 2% w/w neutral sodium Fluoride)

Non-Medicinal Ingredients

Non-Medicinal ingredients:

Purified water, saccharin sodium, hydroxyethyl cellulose, phosphoric acid, yellow 5, blue 1, spearmint oil, peppermint oil, sodium hydroxide


Warnings: KEEP OUT OF REACH OF CHILDREN. For professional use only.

Store at room temperature. Do not expose to excessive heat over 40ºC or 104ºF.

Do not use if seal is broken.

Contact Information

Rx Only in US

Made in USA for: AMD Medicom Inc.
2555 Chemin de l’Aviation,
Pointe -Claire, Quebe, Canada
H9P 2Z2

Questions: 1-800-361-2862

Prinicipal Display Panel

DentiCare Denti-Pro
sodium fluoride gel
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:64778-0236
Route of Administration DENTAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Product Characteristics
Color green Score
Shape Size
Flavor MINT Imprint Code
# Item Code Package Description
1 NDC:64778-0236-1 480 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 11/03/1999
Labeler - AMD Medicom Inc. (256880576)
Registrant - AMD Medicom Inc. (256880576)
AMD Medicom Inc.