SODIUM FLUORIDE- sodium fluoride solution/ drops

Valsts: Amerikas Savienotās Valstis

Valoda: angļu

Klimata pārmaiņas: NLM (National Library of Medicine)

Nopērc to tagad

Produkta apraksts Produkta apraksts (SPC)
27-07-2017

Aktīvā sastāvdaļa:

SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)

Pieejams no:

Mayne Pharma Inc

SNN (starptautisko nepatentēto nosaukumu):

SODIUM FLUORIDE

Kompozīcija:

FLUORIDE ION 0.5 mg in 1 mL

Ievadīšanas:

ORAL

Receptes veids:

PRESCRIPTION DRUG

Ārstēšanas norādes:

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. Sodium Fluoride Drops 0.5 mg 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.

Produktu pārskats:

Sodium Fluoride Drops 0.5 mg is supplied in 50 mL bottles with calibrated dropper, NDC 51862-165-50. TAMPER EVIDENT: Do not accept if printed bottle seal around cap is broken or missing. Accepted Dental Therapeutics, Ed. 40. American Dental Association, Chicago, 1984, p.339-402. Jakush, J, New Fluoride schedule adopted. ADA News, May 16, 1994, p.12,14. Store at controlled room temperature 15˚ to 30˚ C (59˚ to 86˚ F). Manufactured for: Libertas Pharma, Inc. Lawrenceville, GA 30043 Iss. 03/11 165-50         743631

Autorizācija statuss:

unapproved drug other

Produkta apraksts

                                SODIUM FLUORIDE- SODIUM FLUORIDE SOLUTION/ DROPS
MAYNE PHARMA INC
_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._
----------
SODIUM FLUORIDE DROPS 0.5 MG DROPS PEACH FLAVORED
* Conforms to new ADA and AAP guidelines for supplementation.
DOSAGE SCHEDULE * WATER F CONTENT
AGE
0- 0.3 PPM
0.3-0.6 PPM
> 0.6 PPM
6 months to 3 years
0.25 mg F = 1/2 mL = Half dropperful
0
0
3-6 years
0.5 mg F= 1 mL = One dropperful
0.25 mg F= 1/2 mL = Half dropperful
0
6-16 years
1 mg F= 2 mL = Two dropperfuls
0.5 mg F= 1 mL = One dropperful
0
DESCRIPTION
Each mL of Sodium Fluoride Drops 0.5 mg contains 0.5 mg fluoride ion
(F-) from 1.1 mg sodium
fluoride (NaF). For use as a dental caries preventive in pediatric
patients. Sugar-free and saccharin-
free.
ACTIVE INGREDIENTS: Sodium Fluoride 0.11% (w/v).
OTHER INGREDIENTS: Citric acid, methyl paraben, peach flavor, purified
water, red #33, sodium benzoate,
sucralose, yellow #6.
KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.
CLINICAL 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.
INDICATIONS AND USAGE
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. Sodium Fluoride Drops
0.5 mg 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.
CONTRAINDICATIONS
Do not use in areas where drinking water exceeds 0.6 ppm F. Do not
administer to pediatric patients less
than 6 months old.
WARNINGS
(See "CONTRAINDICATIONS" above.
PRECAUTIONS
See ""OVERDOSAGE"" section. Incompatibility of fluorid
                                
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