Label: ANY MI NATURAL MAGIC BB NO.5- allantoin cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated March 15, 2014

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    allantoin


  • INACTIVE INGREDIENT

    water,  cyclomethicone, titanium dioxide, zinc oxide, ethylhexyl methoxycinnamate, panax ginseng root ext, peg-7 dimethicone, propylene glycol, arbutin, bentonite, cetyl peg/ppg-10/1 dimethicone, hexyl laurate, betaine, polymethyl methacrylate, sodium chloride, etc


  • PURPOSE

    whitening
    anti-wrinkle
    sun block


  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    after foundation, apply small amounts to whole face by tapping until it is absorbed to skin completely



  • WARNINGS

    1. if you have any abnormal symptoms as followings, you should discontinue to use this cream.  In case of using continuously, you have to consult to dermatologist because it may make symptoms worse.
    a. red macule, swelling, urtication, and irritation during use
    b. symptoms like above by direct ray
    2. do not use if you have a wound, eczema, and dermatitis to the area where you apply this cream
    3. caution during storing and handling
    a. close the cap after use
    b. keep it to the area where babies and infants cannot reachto
    c. keep it to the area where has not high or low temperature and has no direct ray



  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    ANY MI NATURAL MAGIC BB NO.5 
    allantoin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62695-1001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.0005 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CYCLOMETHICONE (UNII: NMQ347994Z)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ARBUTIN (UNII: C5INA23HXF)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62695-1001-140 mL in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34703/15/2014
    Labeler - K.N.Life Co., Ltd. (688270562)
    Registrant - K.N.Life Co., Ltd. (688270562)
    Establishment
    NameAddressID/FEIBusiness Operations
    K.N.Life Co., Ltd.688270562manufacture(62695-1001)