FDA.reportPublic FDA data

Denti-Care Denti-Pro

Manufacturer
AMD Medicom Inc.
Effective date
2021-01-27
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:54:36

Label at a glance#

ProductDenti-Care Denti-Pro Topical Sodium Fluoride 60 Second
Active ingredientSODIUM FLUORIDE
Label structure6 sections

Dosage and administration

Indications: A topical anti-caries preparation Directions: Following prophylaxis treatment, fill 1/3 of tray with gel Insert tray in the patient’s mouth Have patient bite down lightly for 60 seconds Remove tray and have patient expectorate excess Advise patient not to eat, drink or rinse for 30 minutes after application. Medicinal ingredients: Fluoride ions 1.23% w/w (from 2.72% w/w sodium fluoride)

Label contents#

Full prescribing information#

General Information

DESCRIPTION SECTION

AMD Medicom Inc.

DentiCare Pro-Gel

2.72% Topical Sodium Fluoride Gel

60 Second Application (1.23% fluoride ions)

Strawberry

16.23 fl oz / 480mL

NDC 64778-0219-1

NPN 80008336

RX Only in US

Item code 10021-ST

Indications and Directions

INDICATIONS & USAGE SECTION

Indications: A topical anti-caries preparation

Directions:

  1. Following prophylaxis treatment, fill 1/3 of tray with gel
  2. Insert tray in the patient’s mouth
  3. Have patient bite down lightly for 60 seconds
  4. Remove tray and have patient expectorate excess

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

Medicinal ingredients: Fluoride ions 1.23% w/w (from 2.72% w/w sodium fluoride)

Non-Medicinal Ingredients

INACTIVE INGREDIENT SECTION

Carboxy methyl cellulose sodium, phosphoric acid, water, saccharin sodium, titanium dioxide, red dye, strawberry flavor.

Warnings

WARNINGS AND PRECAUTIONS SECTION

KEEP OUT OF REACH OF CHILDREN. For professional use only. Not recommended for children under 18 months of age.

Store at room temperature. Do not expose to excessive heat over 40°C or 104°F.

Do not use if seal is broken.

Contact Information

SPL UNCLASSIFIED SECTION


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

Questions:1-800-361-2862

www.medicom.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Panel 1Panel 1


DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
sodium fluorideACTIVE INGREDIENT8ZYQ1474W71
fluoride ionACTIVE MOIETYQ80VPU408O1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64778-021964778-0219-1, 64778-0219-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM FLUORIDE8ZYQ1474W7ACTIM

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0d1b0c8e-f4c5-e0f7-e063-6394a90acd5174ad9c0b-2a67-458f-ba1e-aad03e598bdf2023-12-22WarningsExact identifier
spl set id: 74ad9c0b-2a67-458f-ba1e-aad03e598bdf

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.