Label: LANCELL SLIMMING- lanthanum chloride gel

  • 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 August 19, 2011

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  • ACTIVE INGREDIENT

    active ingredient: lanthanum chloride, sphacelaria scoparia extract
  • INACTIVE INGREDIENT

    inactive ingredient:  di-water, morus nigra fruits extract, pronus persica extract, platychadus orientalis extract, marchfire glasswort extract, saccharina japonica extract, butylene glycol, polysorbate 80, phenoxy ethanol, polyacrylate crosspolymer-6, ethanol, bisabol, PEG-60, hydrogenated caster oil, methyl paraben, propyl paraben, flavor
  • PURPOSE

    resolve body fat
  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children
  • INDICATIONS & USAGE

    - apply face and body
    - apply over twice a day each one 4~6 ml or apply sufficient quantity to intended part
    - massage with your hands over 3 minutes until the gel components was soaked through skin
    - using the gel before taking exercise would be more effective
  • WARNINGS

    - for external use only
    - do not swallow
    - keep out of eyes, ears and mouth
  • DOSAGE & ADMINISTRATION

    - remove cellulite from the body
  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    LANCELL SLIMMING 
    lanthanum chloride gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76084-3001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LANTHANUM (UNII: 6I3K30563S) (LANTHANUM - UNII:6I3K30563S) LANTHANUM2.5 mL  in 100 mL
    STYPOCAULON SCOPARIUM (UNII: C4AD0HDH4I) (STYPOCAULON SCOPARIUM - UNII:C4AD0HDH4I) STYPOCAULON SCOPARIUM2 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    MORUS NIGRA FRUIT (UNII: 55W745XH99)  
    PEACH (UNII: 3OKE88I3QG)  
    PLATYCLADUS ORIENTALIS LEAF (UNII: 32E5V7G32B)  
    BUPLEURUM FALCATUM ROOT (UNII: X04E310LUY)  
    PRUNUS MUME FLOWER (UNII: 2N8872050J)  
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ETHANOLAMINE HYDROCHLORIDE (UNII: KKP3YYL02F)  
    POLYETHYLENE GLYCOL 3000 (UNII: SA1B764746)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76084-3001-1200 mL in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/19/2010
    Labeler - MICELLBio Co., Ltd (557803411)
    Registrant - MICELLBio Co., Ltd (557803411)
    Establishment
    NameAddressID/FEIBusiness Operations
    MICELLBio Co., Ltd557803411manufacture