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Fluorbon Drops
Overview
What is Fluorbon Drops?
Perry Fluorabon Drops (0.25 mg Fluoride ion per 0.6 ml) are dye free. Each 0.6 ml contains 0.25 mg of the fluoride ion (F) from 0.55 mg sodium fluoride (NaF). Each 0.6 ml for oral administration contains sodium fluoride equivalent to 0.25 mg of the fluoride ion and the following inactive ingredients:
Purified Water USP, Methylparaben, Propylparaben.
What does Fluorbon Drops look like?
What are the available doses of Fluorbon Drops?
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What should I talk to my health care provider before I take Fluorbon Drops?
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How should I use Fluorbon Drops?
For once daily, self-administered, systemic use as a dental caries preventive in pediatric patients. It has been established that ingestion of fluoridated drinking water (1 ppm F) during the period of tooth development results in a significant decrease in the incidence of dental caries. Perry Fluorabon Drops (0.25 mg Fluoride ion per 0.6 ml) were developed to provide systemic fluoride for use as a supplement in pediatric patients from 6 months to 16 years of age living in areas where the drinking water fluoride content does not exceed 0.6 ppm (F).
Follow the directions for using this medication provided by your doctor. This medicine may be given undiluted or mixed with a non-dairy liquid.
What interacts with Fluorbon Drops?
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What are the warnings of Fluorbon Drops?
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What are the precautions of Fluorbon Drops?
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What are the side effects of Fluorbon Drops?
Allergic rash and other idiosyncrasies have rarely been reported. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.
What should I look out for while using Fluorbon Drops?
Perry Fluorabon Drops (0.25 mg Fluoride ion per .6 ml), are contraindicated when the fluoride content of drinking water is 0.6 ppm (F) or more and should not be administered to pediatric patients under the age of 6 months. Do not administer fluoride (any strength) to pediatric patients under age 6 months.
Prolonged daily ingestion of quantities greater than the recommended amount may result in various degrees of dental fluorosis in pediatric patients under age 6 years, especially if the water fluoridation exceeds 0.6 pm. Read directions carefully before using.
What might happen if I take too much Fluorbon Drops?
Accidental ingestion of large amounts of fluoride may result in acute burning in the mouth and sore tongue. Nausea, vomiting, and diarrhea may occur soon after ingestion (with 30 minutes) and are accompanied by salivation, hematemesis, and epigastric cramping abdominal pain. These symptoms may persist for up to 24 hours. If less than 5 mg sodium fluoride/kg body weight (i.e. less than 2.3 mg sodium fluoride/lb body weight) has been ingested, induce vomiting, give orally soluble calcium (e.g. milk, 5% calcium gluconate, or calcium lactate solution) and immediately seek medical assistance. For accidental ingestion of more than 15 mg sodium fluoride/kg of body weight ( i.e. more than 6.9 mg sodium fluoride/lb of body weight), induce vomiting and seek emergency medical help.
How should I store and handle Fluorbon Drops?
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Clinical Information
Chemical Structure
No Image foundClinical Pharmacology
Sodium fluoride acts systemically (before tooth eruption) and topically (post eruption) by increasing tooth resistance to acid dissolution, by promoting remineralization, and by inhibiting the cariogenic microbial process.
Non-Clinical Toxicology
Perry Fluorabon Drops (0.25 mg Fluoride ion per .6 ml), are contraindicated when the fluoride content of drinking water is 0.6 ppm (F) or more and should not be administered to pediatric patients under the age of 6 months. Do not administer fluoride (any strength) to pediatric patients under age 6 months.Prolonged daily ingestion of quantities greater than the recommended amount may result in various degrees of dental fluorosis in pediatric patients under age 6 years, especially if the water fluoridation exceeds 0.6 pm. Read directions carefully before using.
The use of benzodiazepines, opioids, antihistamines, antipsychotics, anti-anxiety agents, or other CNS depressants (including alcohol) concomitantly with Hydrocodone Bitartrate and Homatropine Methylbromide Tablets may cause an additive CNS depressant effect, profound sedation, respiratory depression, coma, and death and should be avoided (see )
The use of MAO inhibitors or tricyclic antidepressants with hydrocodone preparations may increase the effect of either the antidepressant or hydrocodone.
General:
Please refer to and sections for overdose concerns. Use in pediatric patients blow the age of 6 months is not recommended by current American Dental Association and American Academy of Pediatrics guidelines.
Drug Interactions:
Do not eat or drink dairy products within one hour of fluoride administration. Incompatibility of fluoride with dairy foods has been reported due to formation of calcium fluoride which is poorly absorbed.
Nursing Mothers:
It is not known if fluoride ion is excreted in human milk. However, many drugs are excreted in human mild and caution should be exercised when Perry Fluorabon Drops (.025 mg Fluoride ion per 0.6 ml) are administered to nursing women.
Pediatric Use:
The use of Perry Fluorabon Drops (0.25 mg Fluoride ion per 0.6 ml) as a caries preventative in pediatric age groups 6 months to 16 years is supported by evidence from adequate and well-controlled studies on fluoride supplementation from birth through adolescence.
Geriatric Use:
Allergic rash and other idiosyncrasies have rarely been reported. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.
Reference
This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"
While we update our database periodically, we cannot guarantee it is always updated to the latest version.
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