Pill Identifier App

Triple Vitamin Drops With Fluoride

Generic Name: vitamins a, c, d and fluoride
Dosage Form: oral solution/ drops

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.

TRIPLE-VITAMIN FLUORIDE DROPS 0.25 mg per mL

DESCRIPTION

Percentage of U.S. Recommended Daily Allowance
*
U.S. Recommended Daily Allowance has not been established.
Each 1.0 mL supplies: Children 6 mos to 4 years old
Vitamin A (as Vitamin A Palmitate) 1500 IU 60%
Vitamin C (as Ascorbic Acid) 35 mg 88%
Vitamin D (as Cholecalciferol) 400 IU 100%
Fluoride (as Sodium Fluoride) 0.25 mg *

See INDICATIONS AND USAGE section for use by children 6 months to 6 years of age.

This product does not contain the essential vitamin folic acid.

Active ingredient for caries prophylaxis: Fluoride as sodium fluoride. Does not contain folic acid.

Other Ingredients: Caramel color, cherry flavor, glycerin, methylparaben, polysorbate 80, purified water, sodium benzoate and sodium hydroxide.

Triple Vitamin Drops With Fluoride - Clinical Pharmacology

It is well established that fluoridation of the water supply (1 ppm fluoride) during the period of tooth development leads to a significant decrease in the incidence of dental caries.

Hydroxyapatite is the principal crystal for all calcified tissue in the human body. The fluoride ion reacts with the hydroxyapatite in the tooth as it is formed to produce the more caries-resistant crystal, fluorapatite.

The reaction may be expressed by the equation:1

Ca10(PO4)6(OH)2 + 2F-  Ca10(PO4)6F2 + 2OH-

(Hydroxyapatite)           (Fluorapatite)

Three stages of fluoride deposition in tooth enamel can be distinguished:

  1. Small amounts (reflecting the low levels of fluoride in tissue fluids) are incorporated into the enamel crystals while they are being formed.
  2. After enamel has been laid down, fluoride deposition continues in the surface enamel. Diffusion of fluoride from the surface inward is apparently restricted.
  3. After eruption, the surface enamel acquires fluoride from water, food, supplementary fluoride and smaller amounts from saliva.

INDICATIONS AND USAGE

Supplementation of the diet with vitamins A, C and D.

Triple-Vitamin Fluoride Drops 0.25 mg also provide fluoride for caries prophylaxis.

The American Academy of Pediatrics recommends that children up to age 16, in areas where drinking water contains less than optimal levels of fluoride, receive daily fluoride supplementation.

The American Academy of Pediatrics recommend that infants and young children 6 months to 3 years of age, in areas where drinking water contains less than 0.3 ppm of fluoride, and children 3-6 years of age, in areas where the drinking water contains 0.3 through 0.6 ppm of fluoride, receive 0.25 mg of supplemental fluoride daily which is provided in a full dose (1 mL) of Triple-Vitamin Fluoride 0.25 mg drops. (see Dosage and Administration).

Triple-Vitamin Fluoride 0.25 mg drops supply significant amounts of vitamins A, C and D to supplement the diet, and to help assure that nutritional deficiencies of these vitamins will not develop. Thus, in a single easy-to-use preparation, children obtain essential vitamins and fluoride.

WARNINGS

As in the case of all medications, keep out of reach of children.

Precautions

The suggested dose should not be exceeded since dental fluorosis may result from continued ingestion of large amounts of fluoride.

When prescribing vitamin fluoride products:

  1. Determine the fluoride content of the drinking water.
  2. Make sure the child is not receiving significant amounts of fluoride from other medications and swallowed toothpaste.
  3. Periodically check to make sure that the child does not develop significant dental fluorosis.

Triple-Vitamin and Fluoride Drops 0.25 mg should be dispensed in the original plastic container, since contact with glass leads to instability and precipitation. (The amount of sodium fluoride in the 50 mL size is well below the maximum to be dispensed at one time according to recommendations of the American Dental Association.)

Important Considerations When Using Dosage Schedule:

  • If fluoride level is unknown, drinking water should be tested for fluoride content before supplements are prescribed. For testing of fluoride content, contact the local or state health department.
  • All sources of fluoride should be evaluated with a thorough fluoride history.
  • Patient exposure to multiple water sources can make proper prescribing complex.
  • Ingestion of higher than recommended levels of fluoride by children has been associated with an increase in mild dental fluorosis in developing, unerupted teeth.
  • Fluoride supplements require long-term compliance on a daily basis.

Adverse Reactions

Allergic rash and other idiosyncrasies have been rarely reported.

DOSAGE AND ADMINISTRATION

See following chart. May be dropped directly into mouth with dropper; or mixed with cereal, fruit juice or other food.

Fluoride Ion Level in Drinking Water (ppm)*
*
1.0 ppm = 1 mg/liter
2.2 mg sodium fluoride contains 1 mg fluoride ion.
Age <0.3 ppm 0.3-0.6 ppm >0.6 ppm
Birth - 6 months None None None
6 mos - 3 years 0.25 mg (1 mL) / day None None
3 - 6 years 0.50 mg (2 mL) / day 0.25 mg (1 mL) / day None

HOW SUPPLIED

Triple-Vitamin and Fluoride 0.25 mg drops is available in 50 mL bottles with accompanying calibrated dropper.

RECOMMENDED STORAGE

Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C and 30°C (between 59°F and 86°F). After opening, store away from direct light. Close tightly after each use. Occasional deepening of color has no significant effect on vitamin potency.

REFRIGERATION IS NOT REQUIRED.

SHAKE WELL

REFERENCES

  1. Brudevoid F, McCann HG: Fluoride and caries control - Mechanism of action, in Nizel AE (ed): The Science of Nutrition and its Application in Clinical Dentistry. Philadelphia, WB Saunders Co, 1966, pp 331-347.
  2. American Academy of Pediatrics Committee on Nutrition: Fluoride supplementation, Pediatrics 1986;77:758.
  3. American Dental Association Council on Dental Therapeutics: Accepted Dental Therapeutics, ed 38, Chicago, 1979, p 321.
  4. Hennon DK, Stookey GK, Muhler JC: The clinical anticariogenic effectiveness of supplementary fluoride-vitamin preparations - Results at the end of three years. J Dent Children 1966; 33 January:3-12.
  5. Hennon DK, Stookey GK, Muhler JC: The clinical anticariogenic effectiveness of supplementary fluoride-vitamin preparations - Results at the end of four years. J Dent Children 1967; 34 November;439-443.
  6. Hennon DK, Stookey GK, Muhler JC: The clinical anticariogenic effectiveness of supplementary fluoride-vitamin preparations - Results at the end of five and a half years. Phar and Ther in Dent 1970; 1:1.
  7. Hennon DK, Stookey GK, Beiswanger BB: Fluoride-vitamin supplements: Effects on dental caries and fluorosis when used in areas with suboptimum fluoride in the water supply. J Am Dent Assoc 1977; 95-965.

Manufactured for:
Seton Pharmaceuticals, LLC
Manasquan, NJ 08736
1-800-510-3401

Rev. 02/14

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 0.25 mg label

NDC 13925-170-50

Triple-Vitamin
Drops

With Fluoride

0.25 mg

VITAMINS A, C, D
AND FLUORIDE
SUPPLEMENT DROPS

Rx Only

1.69 FL. OZ. (50 mL)

SETON
PHARMACEUTICALS

TRIPLE-VITAMIN DROPS WITH FLUORIDE 
vitamins a, c, d and fluoride solution/ drops
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:13925-170
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VITAMIN A PALMITATE (VITAMIN A) VITAMIN A 1500 [iU]  in 1 mL
ASCORBIC ACID (ASCORBIC ACID) ASCORBIC ACID 35 mg  in 1 mL
CHOLECALCIFEROL (CHOLECALCIFEROL) CHOLECALCIFEROL 400 [iU]  in 1 mL
SODIUM FLUORIDE (FLUORIDE ION) FLUORIDE ION 0.25 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
METHYLPARABEN  
POLYSORBATE 80  
WATER  
GLYCERIN  
SODIUM BENZOATE  
SODIUM HYDROXIDE  
Product Characteristics
Color BROWN (caramel) Score     
Shape Size
Flavor CHERRY Imprint Code
Contains         
Packaging
# Item Code Package Description
1 NDC:13925-170-50 50 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 04/11/2014
Labeler - Seton Pharmaceuticals (828898002)
Revised: 04/2014
 
Seton Pharmaceuticals
Hide
(web4)