Drug Facts

ISA KNOX WXII PLUS LUMINANT WHITENING EMULSION - atractylodes japonica root lotion
LG Household and Healthcare, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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ATRACTYLODES JAPONICA ROOT 0.055ml/100ml

For external use only.

Keep out of reach of children. Is swallowed, get medical help or contact a Poison Control Center right away.

Keep out of eyes. Rinse with water to remove.

Stop use if a rash or irritation develops and lasts.

ISANKNOX

WXII

Luminant Whitening Emulsion

WXIILuminantWhiteningEmulsion

To whiten the skin.

Use after serum or essence.

For external use only.

Apply evenly to skin.

WATER, CYCLOMETHICONE 5, DIPROPYLENE GLYCOL, GLYCERIN, BUTYLENE GLYCOL, CAPROIC ACID, BETAINE, TROLAMINE, METHYLPARABEN, ETHYLPARABEN, XANTHAN GUM, EDETATE TRISODIUM, FD AND C YELLOW NO 5, FD AND C YELLOW NO 6, DIOSMETIN

ISA KNOX WXII PLUS LUMINANT WHITENING EMULSION
atractylodes japonica root lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:53208-384
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ATRACTYLODES JAPONICA ROOT (ATRACTYLODES JAPONICA ROOT)	ATRACTYLODES JAPONICA ROOT	0.055 mL in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER
CYCLOMETHICONE 5
DIPROPYLENE GLYCOL
GLYCERIN
BUTYLENE GLYCOL
CAPROIC ACID
BETAINE
TROLAMINE
METHYLPARABEN
ETHYLPARABEN
XANTHAN GUM
EDETATE TRISODIUM
FD&C YELLOW NO. 5
FD&C YELLOW NO. 6
DIOSMETIN

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:53208-384-02	1 CONTAINER ( CONTAINER) in 1 BOX	contains a CONTAINER (53208-384-01)
1	NDC:53208-384-01	120 mL in 1 CONTAINER	This package is contained within the BOX (53208-384-02)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/17/2010	01/01/2011

Labeler - LG Household and Healthcare, Inc. (688276187)

Registrant - LG Household and Healthcare, Inc. (688276187)

Establishment
Name	Address	ID/FEI	Operations
LG Household and Healthcare, Inc.		688276187	manufacture

Revised: 05/2012 LG Household and Healthcare, Inc.