Label: SOLMEET DENTI DOCTOR - calcium carbonate paste, dentifrice

  • 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 December 15, 2010

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  • ACTIVE INGREDIENT

    Active Ingredient: Calcium Carbonate, Dibasic Calcium Phosphate Hydrate, Aminocarproic Acid, Aluminium Chlorohydroxy Allantoinate Close
  • INACTIVE INGREDIENT

    Inactive ingredients: calcium carbonate, dibasic calcium phosphate hydrate, amonicaproic acid, aluminium chlorohydroxy allantoinate, glycerine, D-sorbitol, polyethylene glycol-1500, carboxymethylcellulose sodium, sodium lauryl sulfate, methylparaben, xylitol, L-menthol, peppermint oil, yellow no.5, blue no.1, angelica dahurica root extract, phellodendron bark extract, rosin, purified water Close
  • PURPOSE

    for dental care
    Close
  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children Close
  • INDICATIONS & USAGE

    use when is needed Close
  • WARNINGS

    - do not swallow when using this product
    - if more than used for rinsing is accidentally swallowed, get medical helps or contact a poison control center right away Close
  • DOSAGE & ADMINISTRATION

    apply proper amount on your toothbrush Close
  • INGREDIENTS AND APPEARANCE
    SOLMEET DENTI DOCTOR 
    calcium carbonate paste, dentifrice
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:42352-2001
    Route of Administration DENTAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE 15.85 g  in 100 g
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) (PHOSPHATE ION - UNII:NK08V8K8HR) DIBASIC CALCIUM PHOSPHATE DIHYDRATE 0.6 g  in 100 g
    AMINOCAPROIC ACID (UNII: U6F3787206) (AMINOCAPROIC ACID - UNII:U6F3787206) AMINOCAPROIC ACID 0.05 g  in 100 g
    ALCLOXA (UNII: 18B8O9DQA2) (ALCLOXA - UNII:18B8O9DQA2) ALCLOXA 0.05 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SORBITOL (UNII: 506T60A25R)  
    POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    XYLITOL (UNII: VCQ006KQ1E)  
    LEVOMENTHOL (UNII: BZ1R15MTK7)  
    PEPPERMINT (UNII: V95R5KMY2B)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)  
    PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)  
    ROSIN (UNII: 88S87KL877)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:42352-2001-1 120 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 12/15/2010
    Labeler - Solbin Co., Ltd (631099371)
    Registrant - Solbin Co., Ltd (631099371)
    Establishment
    Name Address ID/FEI Business Operations
    Solbin Co., Ltd 631099371 manufacture
    Close