Label: CHIGGER RELIEF EVORA LABS- benzocaine 10% ointment

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 14, 2022

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  • Active ingredient                               Purpose

    Benzocaine 10%                                 Pain Relief

  • PURPOSE

  • Uses

    Temporary releif of pain and itching due to

    • chigger bites
    • red bug bites
    • ticks
    • mosquito bites
  • WarningsFor external use only.

    When using this product avoid contact with eyes.

    Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occure again within a few days.

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Adults and children 2 years of age and older: apply to affected arenot more than 3 to 4 times daily.

    Children under 2 years of age: ask a doctor.

  • Inactive ingredients

    WATER
    PEG-2 STEARATE
    OLEA EUROPAEA (OLIV) FRUIT EXTRACT
    ALOE BARBADENSIS LEAF EXTRACT
    METHYLPARABEN
    DIAZOLIDINYL UREA
    PEPPERMINT OIL
    EUGENIA CARYOPFYLLUS (CLOVE) FLOWER OIL
    PROPYLPARABEN
    CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT
    PEG-8 DIMETHICONE
    ZEA MAYS CORN OIL
    PROPYLENE GLYCOL
    OCTYLDODECANOL
    TOCOPHERYL ACETATE
    ASCORBIC ACID
    RETINYL PALMITATE
    PYRIDOXINE HCL
    CHOLECALCIFEROL
    SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA
    FRAGRANCE
    DISODIUM EDTA
    CAMPHOR

  • QUESTIONS?

    1-888-793-8450

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    CHIGGER RELIEF   EVORA LABS
    benzocaine 10% ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77375-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE10 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PEG-2 STEARATE (UNII: 94YQ11Y95F)  
    BLACK OLIVE (UNII: 2M6QWV94OC)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    CLOVE OIL (UNII: 578389D6D0)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    CHAMOMILE (UNII: FGL3685T2X)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    CORN OIL (UNII: 8470G57WFM)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77375-005-0150 g in 1 CONTAINER; Type 0: Not a Combination Product06/04/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34806/04/2020
    Labeler - Evora Worldwide (081336028)
    Establishment
    NameAddressID/FEIBusiness Operations
    Inspec Solution081030372manufacture(77375-005)
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