ISAKNOX X202 WHITENING SECRET ESSENCE- diosmetin cream

ISAKNOX X202 WHITENING SECRET ESSENCE by

Drug Labeling and Warnings

ISAKNOX X202 WHITENING SECRET ESSENCE by is a Otc medication manufactured, distributed, or labeled by LG Household and Healthcare, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

DIHYDROXYMETHOXYCHALCON 0.065

DIOSMETIN 0.055%

WARNINGS

For external use only.

KEEP OUT OF REACH OF CHILDREN

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

PURPOSE

Whitening functional cosmetic.

WHEN USING

Keep out of eyes. Rinse with water to remove.

INDICATIONS & USAGE

After applying toner, dispense 2-3 amounts and apply gently evenly onto your cheeks, chin, nose, and forehead.

INACTIVE INGREDIENT

WATER, DIPROPYLENE GLYCOL, TRIETHYLHEXANOIN, GLYCERIN, DOCOSANOL, POLYETHYLENE GLYCOL 400, CETOSTEARYL ALCOHOL, CYCLOMETHICONE 5, ALCOHOL, PONCIRUS TRIFOLIATA FRUIT, BETAINE, DIMETHICONE, METHYLPARABEN, TROMETHAMINE, GLYCERYL MONOSTEARATE, PROPYLPARABEN, ETHYLPARABEN, EDETATE TRISODIUM, NIACINAMIDE, PAEONIA LACTIFLORA ROOT, CANNA INDICA ROOT.

DOSAGE & ADMINISTRATION

The Secret-Kit tm capsules, comprising active whitening ingredients and fine whine particles, will burst as the essence gets absorbed, transforming your dull, lifeless complexion into more pure and transparent skin.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ISAKNOX X202 WHITENING SECRET ESSENCE 
diosmetin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53208-531
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIOSMETIN (UNII: TWZ37241OT) (DIOSMETIN - UNII:TWZ37241OT)	DIOSMETIN	0.055 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
GLYCERIN (UNII: PDC6A3C0OX)
DOCOSANOL (UNII: 9G1OE216XY)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
ALCOHOL (UNII: 3K9958V90M)
PONCIRUS TRIFOLIATA FRUIT (UNII: 44445L49J2)
ETHYLPARABEN (UNII: 14255EXE39)
EDETATE TRISODIUM (UNII: 420IP921MB)
NIACINAMIDE (UNII: 25X51I8RD4)
PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
CANNA INDICA ROOT (UNII: BZK836AQFQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53208-531-02	1 in 1 BOX
1	NDC: 53208-531-01	50 mL in 1 CONTAINER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/01/2011

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

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

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