Label: RITE AID PAIN RELIEVING- benzocaine 20%, menthol 0.5% spray

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

Drug Label Information

Updated December 15, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Benzocaine 20%, Menthol 0.5%

  • PURPOSE


    Topical Analgesic

  • INDICATIONS & USAGE

    For the temporary relief of pain and itching associated with sunburn, minor skin irritations, insect bites, scrapes, minor cuts, and minor burns.

  • WARNINGS

    For external use only. Flammable--Keep away from fire or flame. Allergyalert: do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "caine" anesthetics. When using this product avoid contact with eyes. Do not spray in the face or mouth. Use only as directed. Contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120F. Stop use and ask a doctor if condition worsens, if symptoms persist for more than 7 days or clear up and occur again within a few days, itching, rash or irritation develops.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Adults and children 2 years of age and older, apply to the affected area not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor. To use this product, hold the can 6 to 12 inches away from the affected area. Direct spray nozzle towards skin and press the button to activate the spray. To apply to face, spray into palm of hand and gently apply.

  • INACTIVE INGREDIENT

    Acetylated Lanolin Alcohol, Alcohol Denat., Aloe Barbadensis Leaf Extract, Cetyl Acetate, Helianthus Annuus (Sunflower) Seed Oil, PEG-8 Laurate, Polysorbate 85.

  • PRINCIPAL DISPLAY PANEL

    Label

  • INGREDIENTS AND APPEARANCE
    RITE AID PAIN RELIEVING 
    benzocaine 20%, menthol 0.5% spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-1343
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE20 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)  
    ALCOHOL (UNII: 3K9958V90M)  
    CETYL ACETATE (UNII: 4Q43814HXS)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    PEG-8 LAURATE (UNII: 762O8IWA10)  
    POLYSORBATE 85 (UNII: A7F3N56197)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-1343-385 g in 1 CAN; Type 0: Not a Combination Product03/31/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/31/2021
    Labeler - Rite Aid (014578892)
    Registrant - Derma Care Research Labs, LLC (116817470)
    Establishment
    NameAddressID/FEIBusiness Operations
    Derma Care Research Labs, LLC116817470manufacture(11822-1343)