Label: CHIGG AWAY- benzocaine lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 26, 2023

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  • SPL UNCLASSIFIED SECTION

    CVS Itch Relief & Repellent

    Drug Facts

  • Active Ingredient

    Benzocaine 5%

  • Purpose

    Anesthetic

  • Use

    Relieves itching and discomfort due to nonpoisonous insect bites such as chiggers (redbugs), mosquitoes, ticks, fleas, no-see-ums, biting flies, fire ants, bees and wasps; summer’s 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 a rash or irritation develops and consult a doctor. As with all pesticides/drugs,

    keep out of the reach of children.

    In case of accidental ingestion, contact 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 yrs. 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 perspiration.

  • 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, and Triothanolamine..

  • CVS

    PRINCIPAL DISPLAY PANEL Itch Relief & Repellent Relieves itching & Repels Chiggers ( Redbugs) 4 FL OZ (118 mL)

  • PRINCIPAL DISPLAY PANEL

    HEBChigg.jpg

  • INGREDIENTS AND APPEARANCE
    CHIGG AWAY 
    benzocaine lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82645-918
    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)  
    HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%) (UNII: L605B5892V)  
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82645-918-94118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/01/2008
    Labeler - Pharma Nobis, LLC (118564114)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114analysis(82645-918) , manufacture(82645-918) , pack(82645-918) , label(82645-918)
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