Label: AGELESS TOTAL SKIN BLEACHING SERUM- hydroquinone liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 62742-4033-1 - Packager: Allure Labs, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated July 1, 2010
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
INACTIVE INGREDIENTS:
Water, Glycolic Acid, Citric Acid, Phytic Acid, Azelaic Acid, Aloe Barbedensis Leaf Extract, Phyenoxyethanol, Ethylhexylglycerin, Hexylene Glycol, Melaleuca Alternifolia (Tea Trea) Leaf Oil, Xanthan Gum, Mentha Virdis (Spearmint) Oil, Eucaluptus Globulus Leaf Oil, Glycyrrhiza Glabra (Licorice) Root Extract, Pineapple-Coconut Enzyme.
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PRINCIPAL DISPLAY PANEL
Other Information on the back of the container:
(Claims)
An oil-free hydroquinone/glycolic acid serum that gently lightens skin discolorations. Daily application lightens melasma, freckeles and other areas of melanin hyperpigmention.
Paraben-free
Directions:
Apply to cleansed skin morning and evening.
Indications:
Freckles, melasma, post pregnancy pigmentation disorders, hand discolorations.
Distributor:Image International
Palm Beach, FL 33411 USA
www.imageskincare.com
Image of the Product (Front): AGELESS Total Skin Bleaching Serum
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INGREDIENTS AND APPEARANCE
AGELESS TOTAL SKIN BLEACHING SERUM
hydroquinone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4033 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE 20 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4033-1 30 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358 01/01/2010 Labeler - Allure Labs, Inc. (926831603)