Label: LUSTER PREMIUM WHITE PRO LIGHT DENTAL WHITENING SYSTEM- sodium monofluorophosphate kit
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Contains inactivated NDC Code(s)
NDC Code(s): 72805-150-28, 72805-170-13 - Packager: French Transit, Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 January 12, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
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Directions
Adults and children 6 years of age and older Brush teeth thoroughly, preferably after each meal, at least twice daily, or as directed by a dentist or doctor. Children 6 to 12 years Instruct in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision. Children under 6 years Do not use unless directed by a dentist or physician. - Other information
- Inactive ingredients
- Questions?
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PRINCIPAL DISPLAY PANEL - Kit Carton
NEW LOOK!
LUSTER
PREMIUM WHITE®BONUS
1OZ POWER
WHITE PRO™PRO LIGHT
DENTAL WHITENING SYSTEM™6 SHADES IN 30 MINUTES†
CLINICALLY PROVEN
PROFESSIONAL WHITENING TECHNOLOGYREVERSE YEARS OF
STAINS IN 30 MIN.3 EASY
STEPSENAMEL SAFE
GENTLE & SULFATE-FREEDUAL-ENERGY WHITENING LIGHT • 4 AAA BATTERIES
ACCELERINSE 6 FL OZ (177 mL) • STAIN LIFTING SERUM .25 FL OZ (7 mL)
POWER WHITE PRO ANTICAVITY FLUORIDE TOOTHPASTE • MINT • NET WT. 1 OZ (28 g)SATISFACTION GUARANTEED‡
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INGREDIENTS AND APPEARANCE
LUSTER PREMIUM WHITE PRO LIGHT DENTAL WHITENING SYSTEM
sodium monofluorophosphate kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72805-170 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72805-170-13 1 in 1 CARTON 04/01/2018 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 TUBE 28 g Part 2 1 TUBE 177 mL Part 3 1 TUBE 7 mL Part 1 of 3 LUSTER PREMIUM WHITE POWER WHITE PRO
sodium monofluorophosphate pasteProduct Information Item Code (Source) NDC:72805-150 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium Monofluorophosphate (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.88 g in 100 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Calcium Pyrophosphate (UNII: X69NU20D19) Starch, Corn (UNII: O8232NY3SJ) Propylene Glycol (UNII: 6DC9Q167V3) Polyethylene Glycol 600 (UNII: NL4J9F21N9) Hydrogen Peroxide (UNII: BBX060AN9V) Sodium Lauroyl Sarcosinate (UNII: 632GS99618) Carboxymethylcellulose Sodium, Unspecified Form (UNII: K679OBS311) Carbomer Homopolymer Type A (Allyl Pentaerythritol Crosslinked) (UNII: F68VH75CJC) Saccharin Sodium (UNII: SB8ZUX40TY) Butylated Hydroxytoluene (UNII: 1P9D0Z171K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72805-150-28 28 g in 1 TUBE; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part355 04/01/2018 Part 2 of 3 ACCELERINSE
dentifrices (aerosol, liquid, pastes, and powders) pasteProduct Information Route of Administration DENTAL Other Ingredients Ingredient Kind Ingredient Name Quantity INGR Water (UNII: 059QF0KO0R) INGR Glycerin (UNII: PDC6A3C0OX) INGR Polysorbate 20 (UNII: 7T1F30V5YH) INGR Sodium Bicarbonate (UNII: 8MDF5V39QO) INGR Peppermint Oil (UNII: AV092KU4JH) INGR Sodium Carbonate (UNII: 45P3261C7T) INGR Benzalkonium Chloride (UNII: F5UM2KM3W7) INGR Sucralose (UNII: 96K6UQ3ZD4) INGR Alcohol (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 177 mL in 1 TUBE; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date COSMETIC 04/01/2018 Part 3 of 3 STAIN LIFTING SERUM
dentifrices (aerosol, liquid, pastes, and powders) pasteProduct Information Route of Administration DENTAL Other Ingredients Ingredient Kind Ingredient Name Quantity INGR Alcohol (UNII: 3K9958V90M) INGR Methyl Hydrogenated Rosinate (UNII: 13DHA19W9N) INGR Carbamide Peroxide (UNII: 31PZ2VAU81) INGR Zinc Oxide (UNII: SOI2LOH54Z) INGR Hydroxypropyl Cellulose, Unspecified (UNII: 9XZ8H6N6OH) INGR Peppermint Oil (UNII: AV092KU4JH) INGR Menthol, Unspecified Form (UNII: L7T10EIP3A) INGR Sucralose (UNII: 96K6UQ3ZD4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 7 mL in 1 TUBE; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date COSMETIC 04/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part355 04/01/2018 Labeler - French Transit, Ltd. (100044380)