ANY MI NATURAL MAGIC BB NO.7- allantoin cream

Any Mi Natural Magic BB No.7 by

Drug Labeling and Warnings

Any Mi Natural Magic BB No.7 by is a Otc medication manufactured, distributed, or labeled by K.N.Life Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

ANY MI NATURAL MAGIC BB NO.7 
allantoin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62695-2001
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: 62695-2001-1	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(62695-2001)