Label: DUBAI CHOCOLATE FLUORIDE MOUTHWASH- anticavity mouthwash liquid
- NDC Code(s): 83729-120-16
- Packager: SuperMouth, LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 23, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
-
INACTIVE INGREDIENT
INACTIVE INGREDIENTS
Water, Erythritol, Xylitol, *Hydroxamin®
(Nano-Hydroxyapatite, Menaquinone-7
(Vit K2), Cholecalciferol (Vit D3)), Inulin,
Glycerin, Sodium Gluconate, Sodium
Bicarbonate, Natural Flavors**, Methyl-
sulfonylmethane, Natural Benzoic Acid,
Sodium Ascorbate (Vit C), Xanthan Gum.*Patented Formulation
**Flavor only - no actual chocolate or Dubai ingredients used.
- Product Labeling: Dubai Chocolate Fluoride Mouthwash
-
INGREDIENTS AND APPEARANCE
DUBAI CHOCOLATE FLUORIDE MOUTHWASH
anticavity mouthwash liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83729-120 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.002 mg in 10 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ERYTHRITOL (UNII: RA96B954X6) XYLITOL (UNII: VCQ006KQ1E) TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) MENAQUINONE 7 (UNII: 8427BML8NY) CHOLECALCIFEROL (UNII: 1C6V77QF41) INULIN (UNII: JOS53KRJ01) GLYCERIN (UNII: PDC6A3C0OX) SODIUM GLUCONATE (UNII: R6Q3791S76) SODIUM BICARBONATE (UNII: 8MDF5V39QO) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) BENZOIC ACID (UNII: 8SKN0B0MIM) SODIUM ASCORBATE (UNII: S033EH8359) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color gray Score Shape DIAMOND Size Flavor CHOCOLATE (Pistachio Chocolate Flavor) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83729-120-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/17/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 07/17/2025 Labeler - SuperMouth, LLC. (049384038) Registrant - SuperMouth, LLC. (049384038) Establishment Name Address ID/FEI Business Operations Green Star Labs 118673251 manufacture(83729-120)

