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Sodium fluoride 1.1% dental gel mint - Medication Information

Product NDC Code 71085-074
Drug Name

Sodium fluoride 1.1% dental gel mint

Type Brand
Active Ingredients
Sodium fluoride 1.1 g/100g
Route ORAL
Dosage Form GEL
RxCUI drug identifier 392038
Labeler Name IPG PHARMACEUTICALS, INC.
Packages
Package NDC Code Description
71085-074-02 1 tube in 1 carton (71085-074-02) / 200 g in 1 tube
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient 1.1% neutral sodium fluoride

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Use twice a day (morning and evening) in place of regular toothpaste or as recommended by a dentist or a physician. Adults and Children 6 Years of Age and Older : Twist off cap and remove foil seal. Apply at least a1-inch strip of gel onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute. Spit out and rinse mouth thoroughly. Make sure to brush all sensitive areas of the teeth. Dosage form and Strengths : Dental gel containing 1.1% sodium fluoride.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredient Water, Glycerin, Hydrated Silica, Calcium Carbonate, Xylitol, Sorbitol, Xanthan Gum, Flavor, Yucca Shidigera Root Extract, Quillaja Saponaria Bark Extract, Smilax Aristolochiaefolia Root Extract, Dioscorea Villosa Root Extract, Tocopheryl Acetate, Cocamidopropyl Betaine, Benzyl Alcohol.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses This is a fluoride dental gel intended for use as a dental caries preventive in adults and pediatric patients.

Purpose

Information about the drug product’s indications for use.
Sodium Fluoride Dental Gel 1.1% is a flavored, pH neutral 1.1% sodium fluoride that aids in the prevention of dental decay and helps to treat sensitive teeth.

Spl product data elements

Usually a list of ingredients in a drug product.
Sodium Fluoride 1.1% Dental Gel MINT SODIUM FLUORIDE WATER GLYCERIN HYDRATED SILICA CALCIUM CARBONATE XYLITOL SORBITOL XANTHAN GUM YUCCA SCHIDIGERA WHOLE QUILLAJA SAPONARIA BARK SMILAX ARISTOLOCHIIFOLIA ROOT DIOSCOREA VILLOSA ROOT .ALPHA.-TOCOPHEROL ACETATE COCAMIDOPROPYL BETAINE BENZYL ALCOHOL SODIUM FLUORIDE FLUORIDE ION

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Product label image description image description

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
How Supplied/Storage : 7.4 oz (200gm) in plastic tube. Store at room temperature 59-86°F (15-30°C)

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warning Contraindications : Avoid use in patients with known hypersensitivity to fluoride. Do not use in pediatric patients under 6 unless directed by a dentist or physician. Warnings and Precautions: Do no swallow. Keep out of reach of children. Read the prescribing information fully before using this product. If the product is accidentally swallowed in quantities greater than would normally occur with a toothpaste, seek medical help right away. See your dentist if the problem persists or worsens. Do not use this product longer than 4 weeks unless recommended by a dentist or physician. Adverse reactions: To report suspected Adverse reactions , To report suspected adverse reactions, contact IPG Pharmaceuticals at (888) 711-7116 or the FDA at (800) FDA-1088 or www.fda.gov/medwatch.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API