Land: USA
Språk: engelsk
Kilde: NLM (National Library of Medicine)
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)
IQ Dental Supply, LLC
SODIUM FLUORIDE
FLUORIDE ION 5.6 g in 454 g
DENTAL
PRESCRIPTION DRUG
Fluoride Ion 1.23%..............................................Flouride Treatment Gel Available from 2.09% Sodium Fluoride and Hydrofluoric Acid - A stable thixotropic fluoride treatment gel used to help prevent dental decay. - For Professional Use Only. This product is not intended for home or unsupervised use.
unapproved drug other
NRG APF- SODIUM FLUORIDE GEL IQ DENTAL SUPPLY, LLC _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._ ---------- ACTIVE INGREDIENT: PURPOSE: Fluoride Ion 1.23%..............................................Flouride Treatment Gel Available from 2.09% Sodium Fluoride and Hydrofluoric Acid INDICATIONS AND USAGE: A stable thixotropic fluoride treatment gel used to help prevent dental decay. For Professional Use Only. This product is not intended for home or unsupervised use. WARNINGS: Keep out of reach of children. Do not swallow. If product is accidentally swallowed in quantities greater than would normally occur with a treatment gel, seek medical help or contact a Poison Control Center right away. Read directions carefully before using. DOSAGE AND ADMINISTRATION: Shake well before use. This is a one minute or four minute fluoride gel for in-office patient use. It is normally used as a preventative caries treatment two times a year. 1. After thorough prophylaxsis, fill two single or one dual tray, one third full with gel. Air dry teeth and insert trays into the mouth. 2. Instruct patient to bite down lightly but firmly for one minute (80% effectiveness) or four minutes (100% effectiveness). 3. Remove trays. Instruct patient to expectorate any excess gel and not to eat or drink for at least 30 minutes. OTHER INFORMATION: Store at controlled room temperature 59° to 86°F (15°-30°C). Protect from freezing. INACTIVE INGREDIENTS: Citric Acid, FD&C Red #40, FD&C Yellow #5 (tartrazine) as a color additive, Flavor, Magnesium Aluminum Silicate, Phosphoric Acid, Polysorbate 20, Sodium Benzoate, Sodium Saccharin, Titanium Dioxide, Water, Xanthan Gum, Xylitol. NRG APF sodium fluoride gel PRODUCT INFORMATION PRODUCT TYPE HUMAN PRESCRIPTION DRUG ITEM CODE (SOURCE) NDC:42756-1116 ROUTE OF ADMINISTRATION DENTAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH SODIUM FLU Les hele dokumentet