ANY MI NATURAL MAGIC BB NO.5 - allantoin cream 
K.N.Life Co., Ltd.

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.

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Drug Facts

allantoin


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


whitening
anti-wrinkle
sun block


keep out of reach of the children

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



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



for external use only

package label
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)

Revised: 3/2014
Document Id: cab51b1d-a07b-4249-a146-bde1ddb992da
Set id: 89a22711-a05c-41a0-a0c3-4faa3eb43741
Version: 1
Effective Time: 20140315
 
K.N.Life Co., Ltd.