Label: AGELESS TOTAL SKIN BLEACHING SERUM - hydroquinone liquid 

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 07/10

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:
    Hydroquinone: 2%
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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

    Image of the Product



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  • INGREDIENTS AND APPEARANCE
    AGELESS TOTAL SKIN BLEACHING SERUM 
    hydroquinone liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:62742-4033
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HYDROQUINONE (HYDROQUINONE) 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)
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