Label: CAREDO PROFESSIONAL CAVITIES TREATMENT TOOTHPASTES 100G- cavities treatment toothpaste paste, dentifrice
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Contains inactivated NDC Code(s)
NDC Code(s): 72415-231-50 - Packager: Hong Kong Prosthodontics Medicine Limited
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated August 15, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
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Inactive ingredient
calcium carbonate (50%): 50g/package;
glycerol (30%): 30g/package;
deionized water (14.3%): 14.3g/package;
sodium lauryl sulfate (2%): 2g/package;
carboxymethyl cellulose (1%): 1g/package;
edible saccharin sodium (0.1%): 0.1g/package;
spearmint flavoring (1.5%): 1.5g/package;glutamic acid (0.5%): 0.5g/package;
clove oil basil oil (0.1%): 0.1g/package.
- Purpose
- When using
- Do not use
- Stop use
- Ask doctor
- Ask doctor/pharmacist
- Keep out of reach of children
- Questions
- Pregnancy or breast feeding
- Indications & usage
- Dosage & administration
- Dosage forms & strengths
- Warnings
- Package label. Principal display panel
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INGREDIENTS AND APPEARANCE
CAREDO PROFESSIONAL CAVITIES TREATMENT TOOTHPASTES 100G
cavities treatment toothpaste paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72415-231 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM PHOSPHATE, UNSPECIFIED FORM (UNII: 97Z1WI3NDX) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM PHOSPHATE, UNSPECIFIED FORM 0.5 g in 100 g Inactive Ingredients Ingredient Name Strength CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) 1 g in 100 g WATER (UNII: 059QF0KO0R) 14.3 g in 100 g CALCIUM CARBONATE (UNII: H0G9379FGK) 50 g in 100 g SACCHARIN SODIUM (UNII: SB8ZUX40TY) 0.1 g in 100 g SODIUM LAURYL SULFATE (UNII: 368GB5141J) 2 g in 100 g GLYCERIN (UNII: PDC6A3C0OX) 30 g in 100 g BASIL OIL (UNII: Z129UMU8LE) 0.1 g in 100 g SPEARMINT OIL (UNII: C3M81465G5) 1.5 g in 100 g GLUTAMIC ACID (UNII: 3KX376GY7L) 0.5 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72415-231-50 100 g in 1 TUBE; Type 0: Not a Combination Product 07/03/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/03/2018 Labeler - Hong Kong Prosthodontics Medicine Limited (664580884) Registrant - Hong Kong Prosthodontics Medicine Limited (664580884) Establishment Name Address ID/FEI Business Operations Hong Kong Prosthodontics Medicine Limited 664580884 label(72415-231) , manufacture(72415-231)
