Label: MULTI-VITAMIN WITH FLUORIDE- vitamin a, ascorbic acid, cholecalciferol, alpha-tocopherol acetate, thiamine hydrochloride, riboflavin 5-phosphate sodium, cyanocobalamin, niacinamide, pyridoxine hydrochloride and sodium fluoride liquid

  • NDC Code(s): 58657-326-50
  • Packager: Method Pharmaceuticals, LLC
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated December 12, 2023

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  • SPL UNCLASSIFIED SECTION

    Multi-Vitamin Drops with Fluoride 0.5 mg

    Supplemental Facts

    Percentage of U.S. Recommended Daily Allowance
    Each 1.0 mL supplies:Children 6 mos to 4 Years old
    Vitamin A (as Vitamin A Palmitate)1500 IU60%
    Vitamin C (as Ascorbic Acid)35 mg88%
    Vitamin D (as Cholecalciferol)400 IU100%
    Vitamin E (as D-Alpha-Tocopheryl 
    Acid Succinate)
    5 IU50%
    Vitamin B1 (as Thiamine HCl)0.5 mg71%
    Vitamin B2 (as Riboflavin Phosphate Sodium)
    0.6 mg75%
    Vitamin B12 (as Cyanocobalamin)2 mcg67%
    Niacin (as Niacinamide)8 mg89%
    Vitamin B6 (as Pyridoxine HCl)0.4 mg57%
    Fluoride (as Sodium Fluoride)0.5 mg*

    *Daily Value not established.

    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. This product does not contain Folic Acid.

    Other ingredients: Cherry Flavor, Citric Acid Anhydrous, Glycerin, Orange Flavor, Potassium Sorbate, Propylene Glycol, Purified Water, Sodium Benzoate, Sorbitol Solution, Sucralose.

  • 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 hydroxyapatite in the tooth as it is formed to produce the more caries-resistant crystal, fluorapatite.

    The reaction may be expressed by the equation:

    structure

    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.

    Multi-Vitamin Drops with Fluoride 0.5 mg also provides 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 the 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 0.5 mg of supplemental fluoride daily which is provided in a dose of 1 mL of Multi-Vitamin Drops with Fluoride 0.5 mg (See Dosage and Administration).

    Multi-Vitamin Drops with Fluoride 0.5 mg 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.

    Multi-Vitamin Drops with Fluoride 0.5 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 the mouth with dropper; or mixed with cereal, fruit juice or other food.

    Fluoride Ion Level in Drinking Water (ppm)*
    Age<0.3 ppm0.3 - 0.6 ppm>0.6 ppm
    Birth - 6 monthsNoneNoneNone
    6 mos - 3 years0.25 mg (1 mL) / day NoneNone
    3 - 6 years0.50 mg (2 mL) / day0.25 mg (1 mL) / dayNone

    *  1.0 ppm = 1 mg/liter

     2.2 mg sodium fluoride contains 1 mg fluoride ion.

  • HOW SUPPLIED

    Multi-Vitamin and Fluoride 0.5 mg drops is available in 50 mL bottles with accompanying calibrated dropper.

    dropper

  • RECOMMENDED STORAGE

    Store at controlled room temperature 15°-25°C (between 59°F and 77°F). Excursions Permitted. 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, p321.
    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

    Distributed by:
    Method Pharmaceuticals, LLC
    Fort Worth, TX 76118

    877-250-3427

    Rev. 01/17

    Made in the USA

  • PRINCIPAL DISPLAY PANEL

    NDC 58657-326-50

    Multi- Vitamin

    Drops

    With Fluoride

    0.5 mg

    1.69 FL. OZ. (50 mL)

    label

  • INGREDIENTS AND APPEARANCE
    MULTI-VITAMIN WITH FLUORIDE 
    vitamin a, ascorbic acid, cholecalciferol, alpha-tocopherol acetate, thiamine hydrochloride, riboflavin 5-phosphate sodium, cyanocobalamin, niacinamide, pyridoxine hydrochloride and sodium fluoride liquid
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:58657-326
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) (VITAMIN A - UNII:81G40H8B0T) VITAMIN A1500 [iU]  in 1 mL
    ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID35 mg  in 1 mL
    CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41) CHOLECALCIFEROL400 [iU]  in 1 mL
    .ALPHA.-TOCOPHEROL SUCCINATE, D- (UNII: LU4B53JYVE) (.ALPHA.-TOCOPHEROL, D- - UNII:N9PR3490H9) .ALPHA.-TOCOPHEROL SUCCINATE, D-5 [iU]  in 1 mL
    THIAMINE HYDROCHLORIDE (UNII: M572600E5P) (THIAMINE ION - UNII:4ABT0J945J) THIAMINE0.5 mg  in 1 mL
    RIBOFLAVIN 5'-PHOSPHATE SODIUM (UNII: 20RD1DZH99) (FLAVIN MONONUCLEOTIDE - UNII:7N464URE7E) FLAVIN MONONUCLEOTIDE0.6 mg  in 1 mL
    CYANOCOBALAMIN (UNII: P6YC3EG204) (CYANOCOBALAMIN - UNII:P6YC3EG204) CYANOCOBALAMIN2 ug  in 1 mL
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE8 mg  in 1 mL
    PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) (PYRIDOXINE - UNII:KV2JZ1BI6Z) PYRIDOXINE HYDROCHLORIDE0.4 mg  in 1 mL
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorCHERRY, ORANGEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58657-326-501 in 1 BOX02/24/2017
    150 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/24/2017
    Labeler - Method Pharmaceuticals, LLC (060216698)