Label: ANY MI NATURAL MAGIC BB NO.5 - allantoin cream
- NDC Code(s): 62695-1001-1
- Packager: K.N.Life Co., Ltd.
- 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.
Updated March 15, 2014
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- ACTIVE INGREDIENT
- 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
- KEEP OUT OF REACH OF CHILDREN
keep out of reach of the childrenClose
- INDICATIONS & USAGE
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
- DOSAGE & ADMINISTRATION
for external use onlyClose
- INGREDIENTS AND APPEARANCE
ANY MI NATURAL MAGIC BB NO.5
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)