TOPEX 60 SECOND FLUORIDE FOAM  BUBBLE FUN- sodium fluoride aerosol, foam 
TOPEX 60 SECOND FLUORIDE FOAM  GRAPE- sodium fluoride aerosol, foam 
TOPEX 60 SECOND FLUORIDE FOAM  SPEARMINT- sodium fluoride aerosol, foam 
TOPEX 60 SECOND FLUORIDE FOAM  ORANGE CREAM- sodium fluoride aerosol, foam 
TOPEX 60 SECOND FLUORIDE FOAM  STRAWBERRY- sodium fluoride aerosol, foam 
Dentsply LLC. Professional Division Trading as "Sultan Healthcare"

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.

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Topex 60 Second Fluoride Foam

INDICATIONS AND USAGE

Topex® Fluoride Foams are indicated for topical application to teeth to aid in the prevention of dental caries.
The non-acidic nature of Neutral pH (NaF) is recommended for patients with ceramic or composite restorations.

DOSAGE AND ADMINISTRATION

1. Remove cap from can. If this is the first time using can, break the protective shipping tab by gently lifting up the trigger.

2. Shake can thoroughly for at least 10 seconds before each use.

3. Completely invert can and slowly depress trigger to dispense foam into a fluoride tray

4. Air dry teeth thoroughly and insert tray into patient’s mouth. Have patient close into the tray and use a slight chewing motion to ensure interproximal coverage.

5. Leave tray in contact with teeth between 1-4 minutes. Use a saliva ejector during treatment to minimize ingestion of product

6. Remove tray after elapsed time and have patient expectorate. Instruct patient to refrain from drinking, eating, or rinsing for 30 minutes after treatment.

Treatment frequency should not exceed 4 treatments per year.

DOSAGE FORMS AND STRENGTHS

APF topical Foam contains 2.73% sodium fluoride (1.23% fluoride ion).

NaF topical gel contains 2.0% sodium fluoride (0.9% fluoride ion).

CONTRAINDICATIONS

Hypersensitivity to fluoride. Do not use if patient has a known allergy to fluoride or any of the other ingredients in this
product.

WARNINGS AND PRECAUTIONS

Do not swallow. Harmful if swallowed.
Keep out of reach of children.
This product is not intended for home or unsupervised consumer use.
Contents under pressure. Do not puncture or incinerate canister.
Safety and effectiveness below age 3 have not been established. There have been no long-term animal studies with this product to evaluate carcinogenic, mutagenic, or impairment of fertility potential.
Laboratory studies have indicated that repeated use of APF may dull porcelain, composite restorations and sealants.

ADVERSE REACTIONS

Developing teeth of children under age 6 may become permanently discolored if excessive amounts are repeatedly swallowed. The following adverse reactions are possible in individuals hypersensitive to fluoride: eczema, atopic dermatitis, urticarial, gastric distress, headache, and weakness.

OVERDOSAGE

If treatment dose is swallowed (less than 100 mg F ion), administer milk, limewater, or calcium-type antacid. In case of larger doses, use ipecac syrup emetic and immediately seek medical help.Overdose symptoms include nausea, vomiting, diarrhea, and abdominal pain.

DESCRIPTION

Topex® Fluoride Foams are a family of topical fluoride foam products for professional application in trays. The family consists of APF Foam (1.23% fluoride ion at a pH between 3.0-4.5) and Neutral pH Foam (0.9% fluoride ion at a pH between 6.5 -7.5). Topex® Foam Fluoride products do not contain chlorofluorocarbon propellants.

STORAGE AND HANDLING

Store at 20°C - 25°C (68°F - 77°F); excursions permitted between 15°C - 30°C (59°F - 86°F) [See USP Controlled room temperature.]

MANUFACTURED FOR

Manufactured for:
Sultan Healthcare
1301 Smile Way • York, PA 17404 • USA
T oll Free: 800-637-8582 • Phone: 201-871-1232
Fax: 201-871-0321 • www.sultanhealthcare.com

Made in USA

PRINCIPAL DISPLAY PANEL - Strawberry 4.4 oz

strawberry

PRINCIPAL DISPLAY PANEL - Spearmint 4.4 oz

spearmint

PRINCIPAL DISPLAY PANEL - Bubble Fun 4.4 oz

bubble fun

PRINCIPAL DISPLAY PANEL - Grape 4.4 oz

grape

PRINCIPAL DISPLAY PANEL - Orange Cream 4.4 oz

orange cream

TOPEX 60 SECOND FLUORIDE FOAM   BUBBLE FUN
sodium fluoride aerosol, foam
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0699-0152
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION27.3 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CETYL PHOSPHATE (UNII: VT07D6X67O)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
BENZALDEHYDE (UNII: TA269SD04T)  
APAFLURANE (UNII: R40P36GDK6)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorBUBBLE GUM (Bubble Fun) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0699-0152-441 in 1 BOX01/01/1997
1125 g in 1 CAN; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED DRUG OTHER01/01/1997
TOPEX 60 SECOND FLUORIDE FOAM   GRAPE
sodium fluoride aerosol, foam
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0699-0153
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION27.3 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
BENZALDEHYDE (UNII: TA269SD04T)  
APAFLURANE (UNII: R40P36GDK6)  
CETYL PHOSPHATE (UNII: VT07D6X67O)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0699-0153-441 in 1 BOX01/01/199702/12/2018
1125 g in 1 CAN; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED DRUG OTHER01/01/199702/12/2018
TOPEX 60 SECOND FLUORIDE FOAM   SPEARMINT
sodium fluoride aerosol, foam
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0699-0151
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION27.3 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
APAFLURANE (UNII: R40P36GDK6)  
CETYL PHOSPHATE (UNII: VT07D6X67O)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
BENZALDEHYDE (UNII: TA269SD04T)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorMINT (Spearmint) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0699-0151-441 in 1 BOX01/01/1997
1125 g in 1 CAN; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED DRUG OTHER01/01/1997
TOPEX 60 SECOND FLUORIDE FOAM   ORANGE CREAM
sodium fluoride aerosol, foam
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0699-0154
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION27.3 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CETYL PHOSPHATE (UNII: VT07D6X67O)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
BENZALDEHYDE (UNII: TA269SD04T)  
APAFLURANE (UNII: R40P36GDK6)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorORANGE (Orange Cream) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0699-0154-441 in 1 BOX01/01/199701/31/2022
1125 g in 1 CAN; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED DRUG OTHER01/01/1997
TOPEX 60 SECOND FLUORIDE FOAM   STRAWBERRY
sodium fluoride aerosol, foam
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0699-0150
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION27.3 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
CETYL PHOSPHATE (UNII: VT07D6X67O)  
BENZALDEHYDE (UNII: TA269SD04T)  
APAFLURANE (UNII: R40P36GDK6)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorSTRAWBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0699-0150-441 in 1 BOX01/01/1997
1125 g in 1 CAN; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED DRUG OTHER01/01/1997
Labeler - Dentsply LLC. Professional Division Trading as "Sultan Healthcare" (167087753)
Establishment
NameAddressID/FEIBusiness Operations
Sciarra Laboratories, Inc.824900369MANUFACTURE(0699-0151, 0699-0150, 0699-0152, 0699-0153, 0699-0154)

Revised: 1/2024
Document Id: 8c3d7366-d3f7-41c2-a30e-66c7f5976011
Set id: 60dca200-d977-5662-e053-2991aa0ade04
Version: 4
Effective Time: 20240126
 
Dentsply LLC. Professional Division Trading as "Sultan Healthcare"