Label: TID CLEAN CARE- sodium chloride paste, dentifrice
- NDC Code(s): 73666-0560-1, 73666-0560-2
- Packager: Doctor Choi`s Korea Co., LTD.
- Category: HUMAN OTC DRUG LABEL
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 October 7, 2022
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- Official Label (Printer Friendly)
- 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, Potassium Cocoyl Glycinate, Xylitol, Cooling Agent, Poloxamer 407, Sodium Chloride, Jasmine Mint Flavor, Sodium Bicarbonate, Sodium Benzoate, Polyoxyethylene hydrogenated castor oil, Citrus Mint Flavor, Stevioside, Rosmarinus Officinalis (Rosemary) Leaf Extract", Calendula Officinalis Flower Extract, Eucalyptus Globulus Leaf Extract, Aloe Barbadensis Leaf Extract, Taraxacum Officinale (Dandelion) Root Extract", Camellia Sinensis Leaf Extract
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TID CLEAN CARE
sodium chloride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73666-0560 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) Potassium Cocoyl Glycinate (UNII: WZ70FUF22U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73666-0560-2 1 in 1 CARTON 09/01/2022 1 NDC:73666-0560-1 100 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 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(73666-0560)