Label: KISS MY FACE SENSITIVE FLUORIDE-FREE WHITENING - CITRUS MINT- potassium nitrate paste, dentifrice
- NDC Code(s): 74154-015-04
- Packager: Windmill Health Products, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 February 8, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
-
Inactive ingredients
Sorbitol, Glycerin, Hydrated Silica, Water, Xylitol, Aloe Barbadensis Leaf Extract1, Cetraria Islandica (Iceland Moss) Extract, Aesculus Hippocastanum (Horse Chestnut) Seed Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Olea Europaea (Olive) Leaf Extract, Echinacea Angustifolia Extract, Stevia Rebaudiana Extract, Natural Flavor, Mentha Piperita (Peppermint) Oil, Ammonium Glycyrrhizate (Licorice Root Extract), Xanthan Gum, Menthol, Sodium Methyl Cocoyl Taurate, Sodium Lauroyl Sarcosinate, Cellulose Gum, Chlorophyllin-Copper Complex, Potassium Sorbate
- 1
- Organic
- PRINCIPAL DISPLAY PANEL - 127 g Tube Carton
-
INGREDIENTS AND APPEARANCE
KISS MY FACE SENSITIVE FLUORIDE-FREE WHITENING - CITRUS MINT
potassium nitrate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74154-015 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Potassium Nitrate (UNII: RU45X2JN0Z) (Nitrate Ion - UNII:T93E9Y2844) Potassium Nitrate 0.05 g in 1 g Inactive Ingredients Ingredient Name Strength Sorbitol (UNII: 506T60A25R) Glycerin (UNII: PDC6A3C0OX) Hydrated Silica (UNII: Y6O7T4G8P9) Water (UNII: 059QF0KO0R) Xylitol (UNII: VCQ006KQ1E) Aloe Vera Leaf (UNII: ZY81Z83H0X) CETRARIA ISLANDICA WHOLE (UNII: BJ7YPN79A1) HORSE CHESTNUT (UNII: 3C18L6RJAZ) Tea Tree Oil (UNII: VIF565UC2G) OLEA EUROPAEA LEAF (UNII: MJ95C3OH47) Echinacea Angustifolia Whole (UNII: VB06AV5US8) STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876) PEPPERMINT OIL (UNII: AV092KU4JH) Licorice (UNII: 61ZBX54883) Xanthan Gum (UNII: TTV12P4NEE) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) Sodium Methyl Cocoyl Taurate (UNII: JVL98CG53G) Sodium Lauroyl Sarcosinate (UNII: 632GS99618) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) SODIUM COPPER CHLOROPHYLLIN (UNII: 1D276TYV9O) Potassium Sorbate (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74154-015-04 1 in 1 CARTON 02/18/2022 1 127 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 OTC MONOGRAPH NOT FINAL part356 02/18/2022 Labeler - Windmill Health Products, LLC (831136267) Establishment Name Address ID/FEI Business Operations Lornamead 080046418 MANUFACTURE(74154-015)