CLEAR ACTION- hydroquinone cream

CLEAR ACTION by

Drug Labeling and Warnings

CLEAR ACTION by is a Otc medication manufactured, distributed, or labeled by AQUIMPEX SPA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Dermofading Cream Face CLEAR MAXI TONE 5+ specially designed to impart youthful glow and supreme brightness to dull skin with uneven tone. Its action enhances skin luminosity in
as little as few weeks.

Use

Use: spread a thin layer on skin areas to be treated; apply mornings and evenings on perfectly cleansed skin, massaging delicately until complete absorption.

Caution

Caution: For external use only - It contains Hydroquinone - Keep away from eyes - Apply on small surfaces only - In case of allergic symptoms, immediately suspend the application - Do not use on children under 12.

Active Ingredients

ACTIVE INGREDIENTS: Hydroquinone 2.00%

Ingredients

Ingredients: Water, Propylene Glycol, Mineral Oil, Stearic Acid, Palmitic Acid, Glyceryl Stearate, Cetyl Alcohol, Fragrance, Sodium Sulfite, Potassium Cetyl Phosphate, Isopropyl Myristate,
Citric Acid, Lactic Acid, Acrylates/c10-30 Alkyl Acrylate Crosspolymer, Propylparaben, Methylparaben, Brassica Campestris (Rapeseed) Seed Oil, Rosmarinus Officinalis (Rosemary) Leaf Extract. 02/10

STORAGE AND HANDLING

STORE IN A COOL, DRY PLACE - DO NOT EXPOSE TO DIRECT SUNLIGHT - ALWAYS CLOSE AFTER USE.

Use

Use: spread a thin layer on skin areas to be treated; apply mornings and evenings on perfectly cleansed skin, massaging delicately until complete absorption.

Caution

Caution: For external use only - It contains Hydroquinone - Keep away from eyes - Apply on small surfaces only - In case of allergic symptoms, immediately suspend the application - Do not use on children under 12.

Drug Facts

INGREDIENTS AND APPEARANCE

CLEAR ACTION 
hydroquinone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66273-0003
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	10 mL  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ROSEMARY (UNII: IJ67X351P9)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER 934 (UNII: Z135WT9208)
CETYL ALCOHOL (UNII: 936JST6JCN)
STEARIC ACID (UNII: 4ELV7Z65AP)
PALMITIC ACID (UNII: 2V16EO95H1)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
MINERAL OIL (UNII: T5L8T28FGP)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
LACTIC ACID (UNII: 33X04XA5AT)
SODIUM SULFITE (UNII: VTK01UQK3G)
BRASSICA RAPA VAR. RAPA OIL (UNII: N4G8379626)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66273-0003-3	12 in 1 BOX
1	NDC: 66273-0003-2	1 in 1 CELLO PACK
1	NDC: 66273-0003-1	500 mL in 1 JAR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part358A	07/19/2011

Labeler - AQUIMPEX SPA (440651672)

Establishment
Name	Address	ID/FEI	Business Operations
AQUIMPEX SPA		440651672	manufacture