Label: EXENCE WHITE- hydroquinone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 66273-0001-1, 66273-0001-2 - Packager: AQUIMPEX SPA
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated July 12, 2011
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Natural Clear Tone - Lightening
EXENCE WHITE CREAM NATURAL Clear Tone is a rich textured cream to brighten complexion color and gradually reduce freckles and dark spot of the skin caused by age, sun, pregnancy.
Excellent antioxidant cream promoting collagen and elastin synthesis with antimicrobial, anti irritant, anti inflammatory and refreshing actions. - Use
- Caution
- Active Ingredients
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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, Methylparaben, Propylparaben, Brassica Campestris (Rapeseed) Seed Oil, Rosmarinus Officinalis (Rosemary ) Leaf Extract, Hydroxyisohexyl 3-cyclohexene Carboxaldehyde, Hexyl Cinnamal.
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INGREDIENTS AND APPEARANCE
EXENCE WHITE
hydroquinone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66273-0001 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE 4 mL in 200 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ROSEMARY (UNII: IJ67X351P9) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CETYL ALCOHOL (UNII: 936JST6JCN) STEARIC ACID (UNII: 4ELV7Z65AP) PALMITIC ACID (UNII: 2V16EO95H1) CARBOMER 934 (UNII: Z135WT9208) 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:66273-0001-2 12 in 1 BOX 1 NDC:66273-0001-1 200 mL in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part358A 07/12/2011 Labeler - AQUIMPEX SPA (440651672) Establishment Name Address ID/FEI Business Operations AQUIMPEX SPA 440651672 manufacture