Label: DR YOUNG 2P BRIGHTENING UV SUN BLOCK SPF50 PA- arbutin cream

  • 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 October 1, 2009

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:

    Hyaluronic Acid, Scutellaria Baicalensis Root Extract, Beta-Glucan, Phytosterols, Arbutin

  • KEEP OUT OF REACH OF CHILDREN

    CAUTION: Keep away from children.

  • WHEN USING

    HOW TO USE:

    After your basic skin care products, take appropriate amount to put and spread on your entire face.

  • PRINCIPAL DISPLAY PANEL


    Label14c



    LABEL

  • INGREDIENTS AND APPEARANCE
    DR YOUNG 2P BRIGHTENING UV SUN BLOCK SPF50 PA 
    arbutin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43948-5002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN0.5 mL  in 50 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43948-5002-150 mL in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35211/01/2009
    Labeler - The Doctor's Cosmetic Inc (687479378)
    Registrant - The Doctor's Cosmetic Inc (687479378)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Doctor's Cosmetic Inc687479378manufacture
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