Stati Uniti - inglese - NLM (National Library of Medicine)

sancilio & company inc - sodium fluoride (unii: 8zyq1474w7) (fluoride ion - unii:q80vpu408o) - fluoride ion 20 mg in 1 ml - for once weekly use as a dental caries preventative in pediatric patients. do not use in patients with dyaphagia. do not use in pediatric patients under the age of 6 years unless recommended by a dentist or physician.

Stati Uniti - inglese - NLM (National Library of Medicine)

sancilio & company inc - sodium fluoride (unii: 8zyq1474w7) (fluoride ion - unii:q80vpu408o) - fluoride ion 0.5 mg in 1 ml - as a supplemental source of fluoride. it has been established that ingestion of fluoridated drinking water (1 ppm f) during the period of tooth development results in significant decrease in the incidence of dental caries.1 sodium fluoride drops were developed to provide systemic fluoride for use as a supplement in pediatric patients from 6 months to age 3 and older, living in areas where the drinking water fluoride level does not exceed 0.6 ppm f. do not use in areas where drinking water exceeds 0.6 ppm f. do not administer to pediatric patients less than 6 months old.

Stati Uniti - inglese - NLM (National Library of Medicine)

sofie co. dba sofie - sodium fluoride f-18 (unii: 9l75099x6r) (fluoride ion f-18 - unii:4m4we5n2ge) - sodium fluoride f18 injection is indicated for diagnostic positron emission tomography (pet) imaging of bone to defined areas of altered osteogenic activity. none. pregnancy category c any radiopharmaceutical including sodium fluoride f 18 injection has a potential to cause fetal harm. the likelihood of fetal harm depends on the stage of fetal development, and the radionuclide dose. animal reproductive and developmental toxicity studies have not been conducted with sodium fluoride f 18 injection. prior to the administration of sodium fluoride f 18 injection to women of childbearing potential, assess for presence of pregnancy. sodium fluoride f 18 injection should be given to a pregnant woman only if clearly needed. it is not known whether sodium fluoride f 18 injection is excreted into human milk. because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants, a decision should be made whether to interrupt nursing after administration of sodium fluo

Stati Uniti - inglese - NLM (National Library of Medicine)

bamf health inc. - sodium fluoride f-18 (unii: 9l75099x6r) (fluoride ion f-18 - unii:4m4we5n2ge) - sodium fluoride f 18 injection is indicated for diagnostic positron emission tomography (pet) imaging of bone to define areas of altered osteogenic activity. none. pregnancy category c any radiopharmaceutical including sodium fluoride f 18 injection has a potential to cause fetal harm. the likelihood of fetal harm depends on the stage of fetal development, and the radionuclide dose. animal reproductive and developmental toxicity studies have not been conducted with sodium fluoride f 18 injection. prior to the administration of sodium fluoride f 18 injection to women of childbearing potential, assess for presence of pregnancy. sodium fluoride f 18 injection should be given to a pregnant woman only if clearly needed. it is not known whether sodium fluoride f 18 injection is excreted into human milk. because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants, a decision should be made whether to interrupt nursing after administration of sodium fluoride f 18 injection or not to administer sodium fluoride f 18 injection, taking into account the importance of the drug to the mother. the body of scientific information related to radioactive decay, drug tissue distribution, and drug elimination shows that less than 0.01% of the radioactivity administered remains in the body after 24 hours (10 half-lives). to minimize the risks to a nursing infant, interrupt nursing for at least 24 hours. in reported clinical experience in approximately 100 children, weight based doses (2.1 mbq/kg) ranging from 19 mbq-148 mbq (0.5 mci-4 mci) were used. sodium fluoride f 18 was shown to localize to areas of bone turnover including rapidly growing epiphyses in developing long bones. children are more sensitive to radiation and may be at higher risk of cancer from sodium fluoride f 18 injection.

Stati Uniti - inglese - NLM (National Library of Medicine)

dent-mat holdings, llc. - sodium fluoride (unii: 8zyq1474w7) (fluoride ion - unii:q80vpu408o), potassium nitrate (unii: ru45x2jn0z) (nitrate ion - unii:t93e9y2844) - fluoride ion 5 mg in 1 g - fluoridex toothpaste is indicated for use as part of a professional program for the prevention and control of dental caries. do not use in children under 12 years of age unless recommended by a dentist or physician. 8.1 pregnancy pregnancy category b it has been shown that fluoride crosses the placenta of rats, but only 0.01% of the amount administered is incorporated in fetal tissues. animal studies (rats, mice, rabbits) have shown that fluoride is not a teratogen. maternal exposure to 12.2 mg fluoride/kg of body weight (rats) or 13.1 mg/kg of body weight (rabbits) did not affect the litter size or fetal weight and did not increase the frequency of skeletal or visceral malformations. there are no adequate or well controlled clinical studies in pregnant women. however, epidemiological studies conducted in areas with high levels of naturally fluoridated water showed no increase in birth defects. heavy exposure to fluoride during in utero development may result in skeletal fluorosis which becomes evident in chi

Stati Uniti - inglese - NLM (National Library of Medicine)

amd medicom inc. - sodium fluoride (unii: 8zyq1474w7) (fluoride ion - unii:q80vpu408o) - fluoride ion 0.0272 g in 1 ml - indications: topical anti-carie preparation directions: - following prophylaxis treatment, fill 1/3 of tray with gel - insert tray in the patient’s mouth - have patient bite down lightly for 60 seconds - remove tray and have patient expectorate excess. advise patient not to eat, drink or rinse for 30 minutes after application medicinal ingredients: fluoride ions 1.23% w/w (from 2.72% w/w sodium fluoride)

Stati Uniti - inglese - NLM (National Library of Medicine)

amd medicom inc. - sodium fluoride (unii: 8zyq1474w7) (fluoride ion - unii:q80vpu408o) - fluoride ion 0.0272 g in 1 g - indications: topical anti-caries preparation directions: - following prophylaxis treatment, fill ¼ of tray with foam - to dispense, shake bottle vigorously then invert applicator 180° downward to the bottom of the tray - insert tray, have patient bite down lightly for a minimum of 60 seconds, up to 4 minutes - remove tray and have patient expectorate excess advise patient not to eat, drink or rinse for 30 minutes after the treatment medicinal ingredients: fluoride ions 1.23% w/w (from 2.72% w/w sodium fluoride)

Stati Uniti - inglese - NLM (National Library of Medicine)

patterson dental supply inc - sodium fluoride (unii: 8zyq1474w7) (fluoride ion - unii:q80vpu408o) - sodium fluoride 123 mg in 1 g - for topical application to aid in the prevention of dental caries. treatment frequency should not exceed 4 treatments per year. do not use if patient has a known allergy to fluoride or any of the other ingredients in this product.

Stati Uniti - inglese - NLM (National Library of Medicine)

patterson dental supply inc - sodium fluoride (unii: 8zyq1474w7) (fluoride ion - unii:q80vpu408o) - sodium fluoride 123 mg in 1 g - for topical application to aid in the prevention of dental caries. treatment frequency should not exceed 4 treatments per year. do not use if patient has a known allergy to fluoride or any of the other ingredients in this product.

Stati Uniti - inglese - NLM (National Library of Medicine)

amd medicom inc. - sodium fluoride (unii: 8zyq1474w7) (fluoride ion - unii:q80vpu408o) - fluoride ion 0.0272 g in 1 ml - indications: a topical anti-caries preparation directions: - following prophylaxis treatment, fill 1/3 of tray with gel - insert tray in the patient’s mouth - have patient bite down lightly for 60 seconds - remove tray and have patient expectorate excess advise patient not to eat, drink or rinse for 30 minutes after application. medicinal ingredients: fluoride ions 1.23% w/w (from 2.72% w/w sodium fluoride)