Label: L'ECLAT BLANC TOOTHPASTE- silicon dioxide, xylitol, tocopherol acetate paste, dentifrice
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Updated July 9, 2019
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- ACTIVE INGREDIENT
Sorbitol, Purified Water, Glycerin, Sodium Cocoyl Glutamate, Sodium Cellulose Glycolate, Aroma (Fruity Floral), Menthol, Sodium Benzoate, Stevioside, Aloe Vera Leaf Extract, Sodium Hydrogen Carbonate, Eucalyptus Extract, Green Tea Extract, Sage Extract, Chamomile Extract, Rosemary Extract, Silver, Certified Organic Ingredients
- KEEP OUT OF REACH OF CHILDREN
For best results, brush after every meal and whenever you want your breath to be fresh.
Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician).
Children under 2 years: Ask a dentist or physician
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
L'ECLAT BLANC TOOTHPASTE
silicon dioxide, xylitol, tocopherol acetate paste, dentifrice
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73175-030 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Silicon dioxide (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) Silicon dioxide 12.0 g in 100 g Xylitol (UNII: VCQ006KQ1E) (XYLITOL - UNII:VCQ006KQ1E) Xylitol 0.5 g in 100 g .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1) .ALPHA.-TOCOPHEROL ACETATE 0.1 g in 100 g Inactive Ingredients Ingredient Name Strength Sorbitol (UNII: 506T60A25R) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73175-030-02 1 in 1 CARTON 06/01/2019 1 NDC:73175-030-01 100 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/01/2019 Labeler - Toaon Co., Ltd. (694977241) Registrant - Toaon Co., Ltd. (694977241) Establishment Name Address ID/FEI Business Operations DONG IL PHARMS CO., LTD. 557810721 manufacture(73175-030)