ADVANCED LIGHTNING- octinoxate and hydroquinone cream 
CBI Laboratories, Inc

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.

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lightening perfection crème
SKINCARE
INTENSIVE

Drug Facts

Active ingredient

Hydroquinone 2%

Purpose

Skin Lightener

Uses

Warnings

for external use only

for adult use only

When using this product

  • keep out of eyes, rinse with water to remove.

Stop use and ask a doctor if

  • rash or irritation develops and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center right away.

Directions

Inactive ingredients

Aloe Barbadensis Leaf Juice, Ascorbyl Palmitate, Butylene Glycol, Cetyl Alcohol, Citric Acid, Coco-Caprylate/Caprate, Cucumis Sativus (Cucumber) Oil, DEA-Cetyl Phosphate, Diazolidinyl Urea, Dimethicone, Disodium EDTA, Ethylhexyl Methoxycinnamate, Glycerin, Hydrogenated Vegetable Oil, Hydroxyethylcellulose, Lavandula Angustifolia (Lavender) Oil, Magnesium Ascorbyl Phosphate, Methylparaben, Morus Bombycis Root Extract, Propylene Glycol, Propylparaben, Rosa Damascena Flower Water, Saxifraga Sarmentosa Extract, Scutellaria Baicalensis Root Extract, Sodium Bisulfite, Sodium PCA, Sodium Sulfite, Stearic Acid, Tocopherol, Tocopheryl Acetate, Vitis Vinifera (Grape) Fruit Extract, Water (Aqua)

PRINCIPAL DISPLAY PANEL - 56.7 g Carton

lightening perfection crème

SKINCARE
INTENSIVE

Net Wt 2 Oz / 56.7 g

Principal Display Panel - 56.7 g Carton
ADVANCED LIGHTNING 
octinoxate and hydroquinone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24623-042
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE0.02 g  in 1 g
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE0.02 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S)  
WATER (UNII: 059QF0KO0R)  
DIMETHICONE 350 (UNII: 2Y53S6ATLU)  
SODIUM SULFITE (UNII: VTK01UQK3G)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
CUCUMBER (UNII: YY7C30VXJT)  
MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)  
ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24623-042-2256.7 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35207/01/2005
Labeler - CBI Laboratories, Inc (623704368)
Establishment
NameAddressID/FEIBusiness Operations
CBI Laboratories, Inc.623704368MANUFACTURE

Revised: 1/2011
Document Id: bb41140c-ef5b-4c97-96a2-4a0af804f5e1
Set id: f3eea4bf-440b-43cc-96a0-19f543d0adf4
Version: 1
Effective Time: 20110105
 
CBI Laboratories, Inc