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Any Mi Natural Magic BB No.7

Medically reviewed on Mar 15, 2018

Dosage form: cream
Ingredients: ALLANTOIN 0.0005g in 1mL
Labeler: K.N.Life Co., Ltd.
NDC Code: 62695-2001

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 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

ANY MI NATURAL MAGIC BB NO.7 
allantoin cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62695-2001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (ALLANTOIN) ALLANTOIN0.0005 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
CYCLOMETHICONE 
PROPYLENE GLYCOL 
ARBUTIN 
Packaging
#Item CodePackage Description
1NDC:62695-2001-140 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/FEIOperations
K.N.Life Co., Ltd.688270562manufacture(62695-2001)

 
K.N.Life Co., Ltd.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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