Label: QYO QYO TANGERINE BRIGHT MOIST PEELING PACK- kaolin paste

  • 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 January 1, 2019

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  • ACTIVE INGREDIENTS

    KAOLIN 5%

  • PURPOSE

    SKIN PROTECTANT

  • USES

    • Helps prevent and temporarily protects chapped or cracked skin.
  • WARNINGS

    For external use only.

  • WHEN USING

    When using this product • do not get into eyes.

  • STOP USE

    Stop us and ask doctor if • condition worsens • symptoms last
    more than 7 days or clear up and occurs again within a few days.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Apply as needed. • After cleansing your face, apply two spatula of peeling pack and spread evenly on your face. • Wait 10 to 15 minutes. • Massage and deep cleanse your skin before rinsing with luke warm water.

  • Inactive Ingredients

    Water, Sodium lauryl sulfate, Stearic Acid, Glycerin, Volcanic Ash, Buylene Glycol, Potassium Hydroxide, Bentonite, Betaine

  • Other Information

    Protect this product from excessive heat and direct sun.

  • Questions or Comments?

    Call toll free 1-800-311-6680

  • PRINCIPAL DISPLAY PANEL Qyo Qyo Tangerine Bright + Moist Peeling Pack 100mL

    peelingpack

  • INGREDIENTS AND APPEARANCE
    QYO QYO TANGERINE BRIGHT MOIST PEELING PACK 
    kaolin paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71733-108
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KAOLIN (UNII: 24H4NWX5CO) (KAOLIN - UNII:24H4NWX5CO) KAOLIN5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    TANGERINE PEEL (UNII: JU3D414057)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BENTONITE (UNII: A3N5ZCN45C)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71733-108-011 in 1 BOX01/01/2018
    1100 mL in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34701/01/2018
    Labeler - LaLa Co., Ltd. (694617781)
    Establishment
    NameAddressID/FEIBusiness Operations
    LaLa Co., Ltd.694617781manufacture(71733-108)
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