Label: DR.CHOIS TOOTHPASTE FRESH- silica, sodium monofluorophosphate, tetrasodium pyrophosphate, tocopheryl acetate paste, dentifrice
- NDC Code(s): 73666-0520-1, 73666-0520-2
- Packager: Doctor Choi`s Korea Co., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated September 20, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
-
Uses
■ Keep your teeth white and strong.
■ Keep your mouth clean.
■ Refresh the inside of the mouth.
■ Prevents tooth decay caused by fluoride and removes bad breath.
■ Increases aesthetic effect.
■ Removal of plaque (anti-prag)
■ Prevention of gingivitis and periodontitis
■ Prevention of periodontal disease and gum disease
■ Prevention of plaque deposition -
WARNINGS
■ Contains 1000ppm of fluoride.
■ Do not swallow and rinse mouth thoroughly after use
■ If you experience any problems with your gums or mouth during use,
discontinue use and consult your doctor.
■ For children under 6 years of age, use small amounts of toothpaste. And use it
under the supervision of a guardian to avoid sucking or swallowing.
■ Consult a physician or dentist immediately if a child under 6 years old has
swallowed large quantities.
■ Keep out of the reach of children under 6 years of age. - KEEP OUT OF REACH OF CHILDREN
- Directions
- Other Information
- Questions
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INACTIVE INGREDIENTS
Sorbitol, Water, Hydroxyapatite, Cellulose Gum, Xylitol, Sodium Cocoyl, Glutamate, Mentha Pulegium Oil, Citrus Paradisi (Grapefruit) Seed Extract, Foeniculum Vulgare Oil, Cooling Flavor, Chitosan, Camellia Sinensis Leaf Extract, Fruit Mint Flavor, Mild Mint Flavor, Mentha Viridis (Spearmint) Leaf Oil, Pyridoxine HCl, Cinnamomum Zeylanicum bark oil, Sodium Chloride, Eucalyptus Globulus Leaf Oil, Propolis Extract, Chamomilla Recutita(Matricaria) Flower Extract, Aloe Barbadensis Leaf Extract, Chamaecyparis Obtusa Oil, Zinc gluconate, Ubiquinone
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.CHOIS TOOTHPASTE FRESH
silica, sodium monofluorophosphate, tetrasodium pyrophosphate, tocopheryl acetate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73666-0520 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 17.0 g in 100 g Sodium Monofluorophosphate (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.76 g in 100 g SODIUM PYROPHOSPHATE (UNII: O352864B8Z) (PYROPHOSPHORIC ACID - UNII:4E862E7GRQ) SODIUM PYROPHOSPHATE 0.5 g in 100 g .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1) .ALPHA.-TOCOPHEROL ACETATE 0.2 g in 100 g Inactive Ingredients Ingredient Name Strength Sorbitol (UNII: 506T60A25R) Water (UNII: 059QF0KO0R) TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73666-0520-2 1 in 1 CARTON 09/01/2022 1 NDC:73666-0520-1 120 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 unapproved drug other 09/01/2022 Labeler - Doctor Choi`s Korea Co., LTD. (694807399) Registrant - Doctor Choi`s Korea Co., LTD. (694807399) Establishment Name Address ID/FEI Business Operations DONG IL PHARMS CO., LTD. 557810721 manufacture(73666-0520)
