CTx4 Gel 1100 description, usages, side effects, indications, overdosage, supplying and lots more!

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CTx4 Gel 1100

Oral BioTech
Oral BioTech

CariFree® CTx4 Gel 11000.24% w/w sodium fluoride




FULL PRESCRIBING INFORMATION

Sodium Fluoride 0.24%

Anticavity

Aids in the prevention of dental caries (cavities)

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Adults and children 6 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision. Children under 2 years of age: Consult a dentist or doctor.

Glycerin, Hydrated Silica, Hydrogenated Starch Hydrolysate (HSH), Hydroxyapatite, Hydroxyethyl Cellulose, Menthol (Mint only), Natural Flavors, Artificial Flavors (Citrus and Grape only) Polysorbate 20, Potassium Sorbate, Saccharin, Sodium Benzoate, Sodium Bicarbonate, Sodium Hydroxide, Sodium Lauryl Sulfate, Water, Xylitol

CTx4 Gel 1100

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CTx4 Gel 1100

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CTx4 Gel 1100

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CTx4 Gel 1100

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CTx4 Gel 1100

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CTx4 Gel 1100

CTx4 Gel 1100

sodium fluoride GEL, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:61578-203
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 1100 ug

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
HYDRATED SILICA
MALTITOL
TRIBASIC CALCIUM PHOSPHATE
HYDROXYETHYL CELLULOSE (3000 CPS AT 1%)
MENTHOL
POLYSORBATE 20
POTASSIUM SORBATE
SACCHARIN
SODIUM BENZOATE
SODIUM BICARBONATE
SODIUM HYDROXIDE
SODIUM LAURYL SULFATE
water
Xylitol

Product Characteristics

Color
white (opaque)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61578-203-01 56.699 in 1 TUBE, WITH APPLICATOR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2012-05-01


CTx4 Gel 1100

sodium fluoride GEL, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:61578-204
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 1100 ug

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
HYDRATED SILICA
MALTITOL
TRIBASIC CALCIUM PHOSPHATE
HYDROXYETHYL CELLULOSE (3000 CPS AT 1%)
POLYSORBATE 20
POTASSIUM SORBATE
SACCHARIN
SODIUM BENZOATE
SODIUM BICARBONATE
SODIUM HYDROXIDE
SODIUM LAURYL SULFATE
water
Xylitol

Product Characteristics

Color
white (opaque)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61578-204-01 56.699 in 1 TUBE, WITH APPLICATOR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2012-05-01


CTx4 Gel 1100

sodium fluoride GEL, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:61578-207
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 1100 ug

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
HYDRATED SILICA
MALTITOL
TRIBASIC CALCIUM PHOSPHATE
HYDROXYETHYL CELLULOSE (3000 CPS AT 1%)
POLYSORBATE 20
POTASSIUM SORBATE
SACCHARIN
SODIUM BENZOATE
SODIUM BICARBONATE
SODIUM HYDROXIDE
SODIUM LAURYL SULFATE
water
Xylitol

Product Characteristics

Color
white (opaque)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61578-207-01 56.699 in 1 TUBE, WITH APPLICATOR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2012-05-01


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Be sure to consult your doctor before taking any medication!
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