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Name:Advanced Lightning
Manufacturer:Cbi Laboratories, Inc
Category:Over-the-counter (OTC) Marketed Drugs


lightening perfection crème SKINCARE INTENSIVE

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

  • 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

Principal Display Panel - 56.7 g Carton

ADVANCED LIGHTNING 
octinoxate and hydroquinone cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:24623-042
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OCTINOXATE (OCTINOXATE) OCTINOXATE 0.02 g  in 1 g
HYDROQUINONE (HYDROQUINONE) HYDROQUINONE 0.02 g  in 1 g
Inactive Ingredients
Ingredient Name Strength
GLYCERIN  
ALOE VERA LEAF  
CETYL ALCOHOL  
DIETHANOLAMINE CETYL PHOSPHATE  
WATER  
DIMETHICONE 350  
SODIUM SULFITE  
DIAZOLIDINYL UREA  
ALPHA-TOCOPHEROL ACETATE  
STEARIC ACID  
ASCORBYL PALMITATE  
SODIUM METABISULFITE  
CITRIC ACID MONOHYDRATE  
EDETATE DISODIUM  
SODIUM PYRROLIDONE CARBOXYLATE  
CUCUMBER  
MAGNESIUM ASCORBYL PHOSPHATE  
ROSA DAMASCENA FLOWER OIL  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:24623-042-22 56.7 g in 1 JAR None

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 Operations
CBI Laboratories, Inc. 623704368 MANUFACTURE

Revised: 01/2011 CBI Laboratories, Inc



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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