Label: SG PLUS REPELLENT AROMA MIST- icaridin liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 7, 2019

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  • Active Ingredients

    Icaridin (7%)

  • Purpose

    Insect Repellent

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Uses

    Helps to repel insects

  • Directions

    Apply on skin as needed. Re-apply when it is need. After returns home, rinse with water and soap.

  • Warnings

    For external use only

    Do not use when skin is red, inflamed, irritated, or painful

    When using this product do not apply on sensitive parts of the body avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water do not apply directly to wound or open cut Stop use and ask a doctor if Rash or irritation on skin develops and lasts

  • Inactive Ingredients

    Ethanol, Castor oil ethoxylate, Sandalwood oil, Orange oil, Clary oil, Lavender oil, Pinus sylvestris leaf oil, Water

  • SG Plus Repellent Aroma Mist

    aroma mist

  • INGREDIENTS AND APPEARANCE
    SG PLUS REPELLENT AROMA MIST 
    icaridin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71487-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ICARIDIN (UNII: N51GQX0837) (ICARIDIN - UNII:N51GQX0837) ICARIDIN2.1 g  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    SANDALWOOD OIL (UNII: X7X01WMQ5F)  
    CLARY SAGE OIL (UNII: 87L0D4U3M0)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71487-101-021 in 1 PACKAGE06/27/2017
    1NDC:71487-101-0130 mL in 1 CYLINDER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/27/2017
    Labeler - HANKOOK SAMGONG CO.,LTD (687756544)
    Registrant - HANKOOK SAMGONG CO.,LTD (687756544)
    Establishment
    NameAddressID/FEIBusiness Operations
    HANKOOK SAMGONG CO.,LTD687756544manufacture(71487-101)