Label: CHIGG AWAY- benzocaine lotion

  • NDC Code(s): 82895-857-05
  • Packager: Westlake HB Pharma LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 26, 2023

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  • SPL UNCLASSIFIED SECTION

    Chigg Away

    Drug Facts

  • Active Ingredient

    Benzocaine 5%

  • Purpose

    Anesthetic

  • Uses

    Relieves itching and discomfort due to nonpoisonous insect bites such as chiggers (redbugs), mosquitoes, ticks, and fleas, no-see-ums, biting flies, fire ants, bees and wasps; swimmers itch.

  • Warnings

    For external use only. 

    Keep away from eyes or other mucous membranes. Not for prolonged use. For use on intact skin only. Do not use on children younger than 2 yrs.

    When using this product 

    discontinue use if the condition persists or if rash or irritation develops and consult a doctor. As with all pesticides/drugs,

    keep out of reach of children.

    In case of accidental ingestion, contact a physician or poison control center at once.  

  • Directions

    • As an anti-itch: Adults and children 2 yrs. of age and over: apply topically and rub well as needed. Children under 2 years of age: Do not use.
    • As an insect (chigger) repellent: Apply around feet, ankles, waist and to skin under all areas of tight clothing and around all openings in outer clothing. Reapply after heavy respiration.
  • Other Information

    • Disposal: Do not reuse bottle. Rinse thoroughly before discarding.
  • Inactive Ingredient

    Cetyl Alcohol, Glycerin, Glyceryl Stearate, Hydroxyethyl Cellulose, Isopropyl Alcohol, Methylparaben, Petrolatum, Propylparaben, Purified Water, Sodium Lauryl Sulfate, Stearic Acid, Sulfur, Triethanolamine..

  • PRINCIPAL DISPLAY PANEL

    Chigg Stop 2022

    NDC 86000-857-05

    CHIGG

    STOP

    RELIEVES ITCHING

    REPELS CHIGGERS

    4 FL OZ

    (118 ML)

  • INGREDIENTS AND APPEARANCE
    CHIGG AWAY 
    benzocaine lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82895-857
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SULFUR (UNII: 70FD1KFU70)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%) (UNII: L605B5892V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82895-857-05118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/23/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01706/23/2022
    Labeler - Westlake HB Pharma LLC (081176855)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114analysis(82895-857) , pack(82895-857) , manufacture(82895-857) , label(82895-857)
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