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

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  • ACTIVE INGREDIENT

    allantoin


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  • 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


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  • PURPOSE

    whitening
    anti-wrinkle
    sun block


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  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

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  • INDICATIONS & USAGE

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



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  • 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



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  • DOSAGE & ADMINISTRATION

    for external use only

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  • INGREDIENTS AND APPEARANCE
    ANY MI NATURAL MAGIC BB NO.5 
    allantoin cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:62695-1001
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.0005 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CYCLOMETHICONE (UNII: NMQ347994Z)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ARBUTIN (UNII: C5INA23HXF)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:62695-1001-1 40 mL in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 03/15/2014
    Labeler - K.N.Life Co., Ltd. (688270562)
    Registrant - K.N.Life Co., Ltd. (688270562)
    Establishment
    Name Address ID/FEI Business Operations
    K.N.Life Co., Ltd. 688270562 manufacture(62695-1001)
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