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Dawnmist fluoride - Medication Information

Product NDC Code 65517-2017
Drug Name

Dawnmist fluoride

Type Brand
Active Ingredients
Sodium fluoride .22 g/100g
Route DENTAL
Dosage Form PASTE
RxCUI drug identifier 245598
Application Number M022
Labeler Name Dukal LLC
Packages
Package NDC Code Description
65517-2017-0 78 g in 1 tube (65517-2017-0)
65517-2017-1 17 g in 1 tube (65517-2017-1)
65517-2017-2 24 g in 1 tube (65517-2017-2)
65517-2017-3 43 g in 1 tube (65517-2017-3)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Sodium Fluoride 0.22%

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 Adults and children 2 years and older: Brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist or physician. Children under 6 years: To minimize swallowing, use a peas sized amount and supervisor brushing until good habits are established. Children under 2 years: Ask a dentist or physician

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredient Sorbitol, Water, Silica, Sodium Lauryl Sulphate, PEG1500, Flavor, Carboxymethyl Cellulose, Sodium Benzoate, Sodium Saccharin

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.
Use Aids in the prevention of dental cavities

Purpose

Information about the drug product’s indications for use.
Purpose Anticavity

Spl product data elements

Usually a list of ingredients in a drug product.
DAWNMIST FLUORIDE SODIUM FLUORIDE WATER SORBITOL SILICON DIOXIDE SODIUM LAURYL SULFATE POLYETHYLENE GLYCOL 1500 CARBOXYMETHYLCELLULOSE SODIUM BENZOATE SACCHARIN SODIUM 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.
Principal Display Panel - DawnMist Gel Fluoride Toothpaste 2.75 oz Tube Label DawnMist ® NDC: 65517-2017-0 ORAL CARE Gel Fluoride Toothpaste CAVITY FIGHTING FORMULA FRESH MINT FLAVOR 2.75 OZ. (78 g) Principal Display Panel - DawnMist Gel Fluoride Toothpaste 2.75 oz Tube Label

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.
DawnMist Gel Fluoride Toothpaste

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children under 6 years of age If you accidently swallow more than used for brushing seek professional assistance or contact a Poison Control immediately

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:

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