Label: TITAD FRESH BREATH PLUS TOOTH- sodium monofluorophosphate paste, dentifrice
- NDC Code(s): 50555-200-01, 50555-200-02, 50555-200-03, 50555-200-04
- Packager: KMPHARMACEUTICAL CO.,LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive ingredients
Sorbitol, Water, Silica, Hydrated Silica, Glycerin, Flavor, Sodium PCA, Cellulose Gum, Sodium Cocoyl Glutamate, Xylitol, Tetrasodium pyrophosphate, Lauramidopropyl Betaine, Stevia Rebaudiana Extract, Sodium Bicarbonate, Scutellaria Baicalensis Root Extract, Salvia Officinalis (Sage) Extract, Camellia Sinensis Leaf Extract, Tocopheryl Acetate, Menthol, Myrrh Tinc, Chamomile tincture, Rhatany tincture, Chamomilla Recutita (Matricaria) Extract
Fragrance allergen : D-Limonene, Eugenol, Isoeugenol, Linalool
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
DOSAGE & ADMINISTRATION
Directions
■ 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 2 to 6 years : use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)
■ children under 2 years : ask a dentist or physician
- OTHER SAFETY INFORMATION
- QUESTIONS
- TITAD FRESH BREATH PLUS TOOTHPASTE 100g
- TITAD FRESH BREATH PLUS TOOTHPASTE 20g
-
INGREDIENTS AND APPEARANCE
TITAD FRESH BREATH PLUS TOOTH
sodium monofluorophosphate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50555-200 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.76 g in 100 g Inactive Ingredients Ingredient Name Strength XYLITOL (UNII: VCQ006KQ1E) TETRASODIUM PYROPHOSPHATE (UNII: O352864B8Z) SORBITOL (UNII: 506T60A25R) GLYCERIN (UNII: PDC6A3C0OX) CELLULOSE GUM (UNII: K679OBS311) STEVIA REBAUDIANA WHOLE (UNII: 6U422Y08O2) CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0) MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) LIMONENE, (+)- (UNII: GFD7C86Q1W) WATER (UNII: 059QF0KO0R) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) SAGE (UNII: 065C5D077J) ISOEUGENOL (UNII: 5M0MWY797U) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG) LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233) SODIUM BICARBONATE (UNII: 8MDF5V39QO) EUGENOL (UNII: 3T8H1794QW) HYDRATED SILICA (UNII: Y6O7T4G8P9) SODIUM PCA (UNII: 469OTG57A2) LINALOOL (UNII: D81QY6I88E) MENTHOL (UNII: L7T10EIP3A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50555-200-02 1 in 1 CARTON 10/01/2024 1 NDC:50555-200-01 100 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:50555-200-04 1 in 1 CARTON 10/01/2024 2 NDC:50555-200-03 20 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 Drug M021 10/01/2024 Labeler - KMPHARMACEUTICAL CO.,LTD (689850153) Establishment Name Address ID/FEI Business Operations KMPHARMACEUTICAL Co.,Ltd. 689850153 manufacture(50555-200)
