ADVANCED LIGHTNING- octinoxate and hydroquinone cream

Advanced Lightning by

Drug Labeling and Warnings

Advanced Lightning by is a Otc medication manufactured, distributed, or labeled by CBI Laboratories, Inc, CBI Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Hydroquinone 2%

Purpose

Skin Lightener

Uses

• helps fade skin discoloration.
• helps even pigmentation.
• use regularly at night.

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

• Apply thin layer on affected areas after cleansing.
• Follow with moisturizer.
• Wear sunscreen daily.

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

INGREDIENTS AND APPEARANCE

ADVANCED LIGHTNING 
octinoxate and hydroquinone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24623-042
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.02 g  in 1 g
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	0.02 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24623-042-22	56.7 g in 1 JAR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	07/01/2005

Labeler - CBI Laboratories, Inc (623704368)

Establishment
Name	Address	ID/FEI	Business Operations
CBI Laboratories, Inc.		623704368	MANUFACTURE