Label: DR.CHOIS CLEANER PLUS TOOTHPASTE- sodium chloride paste, dentifrice
- NDC Code(s): 73666-0590-1, 73666-0590-2
- Packager: Doctor Choi`s Korea Co., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated April 16, 2024
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- ACTIVE INGREDIENTS
- PURPOSE
- Uses
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WARNINGS
■ Be careful not to swallow, and rinse your mouth thoroughly after use.
■ If an abnormality occurs such as damage to the gums or mouth due to the use of this toothpaste, stop using it and consult a doctor or dentist
■When used by children under the age of 6, use a small amount of toothpaste about the size of a pea per serving, and use under the guidance of a guardian to avoid sucking or swallowing.
■If a child under the age of 6 swallows a large amount, consult a doctor or dentist immediately.
■Keep out of reach of children under the age of 6 - KEEP OUT OF REACH OF CHILDREN
- Directions
- Other Information
- Questions
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INACTIVE INGREDIENTS
Water, Glycerin, Xylitol, Rosmarinus Officinalis Leaf Extract, PEG-40 Hydrogenated Castor Oil, Sodium Benzoate, Poloxamer 407, Stevioside, Mentha Pulegium Oil, Sodium Cocoyl Glutamate, Sodium Lauroyl Sarcosinate, Aloe Barbadensis Leaf Extract, Eucalyptus Globulus Leaf Extract, Salvia Officinalis Leaf Extract, Menthol, Eucalyptus Globulus Leaf Oil, Sodium Citrate, Phytoncide, Zinc Gluconate, Citric Acid
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.CHOIS CLEANER PLUS TOOTHPASTE
sodium chloride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73666-0590 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium Chloride (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) Sodium Chloride 0.7 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Xylitol (UNII: VCQ006KQ1E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73666-0590-2 1 in 1 CARTON 04/01/2024 1 NDC:73666-0590-1 100 mL 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 04/01/2024 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(73666-0590)