FDA Label for Auraglow Daily
View Indications, Usage & Precautions
Auraglow Daily Product Label
The following document was submitted to the FDA by the labeler of this product Auraglow Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Other
Drug Facts
Otc - Active Ingredient
Active ingredient
Sodium fluoride 0.243%
(0.15% w/v fluoride ion)
Otc - Purpose
Purpose Anticavity
Indications & Usage
Use Aids in prevention of dental cavities.
Warnings
Warnings
Otc - Keep Out Of Reach Of Children
Keep out of reach of children under 6 years of age.
If more than used for brushing is accidentally swallowed, get
medical help or contact a Poison Control Center right away.
Dosage & Administration
Directions
• Adults and children 2 years of age and older:
Brush teeth thouroughly, preferably after each meal or
at least twice a day, or as directed by a dentist or doctor.
• Instruct children under 6 years of age in good brushing
and rinsing habits (to minimize swallowing). • Supervise
children as necessary until capable of using without supervision.
• Children under 2 years of age: Consult a dentist or doctor.
Inactive Ingredient
Inactive Ingredients
Deionized water, sorbitol, hydrated silica, xylitol,
glycerin, polyethylene glycol, sodium methyl
cocoyl taurate, flavor, cellulose gum, dimethicone,
monosodium phosphate, stevia, sodium benzoate
Package Labeling
Auraglow
Daily
Toothpaste
Strengthens Teeth
and prevents cavities.
_____________________
Wintergreen
CONTAINS FLUORIDE
_____________________
NET WT 4.0 OZ (113G)
Distr. by Auraglow LLC, Stamford, CT 06901
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