Label: BLANX ADVANCED WHITENING- sodium monofluorophosphate, sodium fluoride paste
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Contains inactivated NDC Code(s)
NDC Code(s): 70781-004-01 - Packager: Coswell Spa
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 4, 2019
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Ingredients:
Aqua, Glycerin, Hydrated Silica, Sorbitol, Silica, Cellulose Gum, Aroma, Xylitol, Cetraria Islandica Extract, Sodium Monofluorophosphate, Sodium Fluoride, Sodium Saccharin, Sodium Myristoyl Sarcosinate, Sodium Methyl Cocoyl Taurate, Sodium Benzoate, Phenoxyethanol, Benzyl Alcohol, Eugenol, Limonene, CI 77891.
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PURPOSE
Non-Abrasive Whitening Toothpaste
Advanced Whitening
Cleans, protects and whitens
For daily use
Complete dental care with Arctic Lichen for natural whitening
BlanX Whitening toothpaste containing Arctic Lichen cleans without abrasiveness, restoring the teeth's original whiteness day by day without harming tooth enamel. Arctic Lichen attacks the bacteria that cause plaque, tartar and discolouring of the teeth.
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- DOSAGE & ADMINISTRATION
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BLANX ADVANCED WHITENING
sodium monofluorophosphate, sodium fluoride pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70781-004 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.08 g in 100 g SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.4 g in 100 g Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) XYLITOL (UNII: VCQ006KQ1E) SODIUM MYRISTOYL SARCOSINATE (UNII: J07237209D) EUGENOL (UNII: 3T8H1794QW) LIMONENE, (+)- (UNII: GFD7C86Q1W) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) BENZYL ALCOHOL (UNII: LKG8494WBH) PHENOXYETHANOL (UNII: HIE492ZZ3T) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM BENZOATE (UNII: OJ245FE5EU) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) GLYCERIN (UNII: PDC6A3C0OX) CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) HYDRATED SILICA (UNII: Y6O7T4G8P9) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70781-004-01 75 g in 1 TUBE; Type 0: Not a Combination Product 04/26/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 04/26/2017 Labeler - Coswell Spa (429512304) Establishment Name Address ID/FEI Business Operations Incos Cosmeceutica Industriale Srl 434933032 manufacture(70781-004)