HOME CARE FLUORIDE- stannous fluoride gel 
Dental Technologies, Inc.

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DTI Stannous - Bubble Gum

Active ingredient

Stannous Fluoride 0.4%

(0.12% w/v fluoride ion)

Purpose

Anticavity

Uses

Helps aid in the prevention of dental cavities.

Warnings

This is an anticavity fluoride preventive treatment gel, not a toothpaste.

Read directions carefully before using.

When using this product

it may produce surface staining of the teeth. Adequate tooth brushing may prevent these stains which are not harmful or permanent and may be removed by your dentist.

Keep out of reach of children.

If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Do not use if the foil seal under the cap is torn, cut or missing.

Inactive ingredients

Ascorbic Acid, Carbomer, Citric Acid, Flavor, Glycerin, Triethanolamine

Questions or comments?

1.800.835.0885 or 847.677.5500

Principal Display Panel

alpha-dent®

HOME CARE

FLUORIDE GEL

0.4% STANNOUS FLUORIDE

AIDS IN THE

PREVENTION

OF DENTAL CAVITIES

BUBBLE GUM

REF 004.0202.001

NET WEIGHT - 4.3 oz. (121.9g)

DENTAL

TECHNOLOGIES

6901 N HAMLIN AVENUE

LINCOLNWOOD, ILLINOIS 60712 USA

www.dentaltech.com

Stannous_bubblegum_image.jpg

HOME CARE FLUORIDE 
stannous fluoride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55346-0402
Route of AdministrationDENTAL, ORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STANNOUS FLUORIDE (UNII: 3FTR44B32Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.969 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)  
Product Characteristics
Color    Score    
ShapeSize
FlavorBUBBLE GUM (Bubble Gum) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55346-0402-1121.9 g in 1 TUBE; Type 0: Not a Combination Product12/31/1999
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02112/31/1999
Labeler - Dental Technologies, Inc. (148312838)
Registrant - Dental Technologies, Inc. (148312838)
Establishment
NameAddressID/FEIBusiness Operations
Dental Technologies, Inc.148312838manufacture(55346-0402) , label(55346-0402) , pack(55346-0402)

Revised: 2/2024
Document Id: 10bd16c6-e578-4a2c-e063-6294a90aa763
Set id: 51f1d84c-809a-4c96-a117-7a8d8aa1e6b4
Version: 8
Effective Time: 20240206
 
Dental Technologies, Inc.