Label: DEEP COVER BUG BITE RELIEF- benzocaine ointment

  • NDC Code(s): 84806-147-03
  • Packager: Morrisons Outdoors, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 21, 2024

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  • ACTIVE INGREDIENT

    Benzocaine 10%

  • PURPOSE

    Pain Relief

  • DOSAGE & ADMINISTRATION

    Uses: for the temporary relief of pain and itching associated with chigger bites, red bug bites, ticks, and mosquito bites.

  • WARNINGS

    For external use only.

    When using this product avoid contact with eyes. Stop use and ask a doctor if the condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days.

  • KEEP OUT OF REACH OF CHILDREN

    In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

  • INDICATIONS & USAGE

    Adults and children 2 years and older: apply to the affected area, not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor.

  • INACTIVE INGREDIENT

    Water, PEG-2 Stearate, Olea Europaea (Olive) Fruit Extract, Mentha Piperita (Peppermint) Oil, Aloe Barbadensis Leaf Extract, Camphor, Eugenia Caryophyllus (Clove) Flower Oil, Chamomilla Recutita (Matricaria) Flower Extract, Propylene Glycol, Tocopheryl Acetate, Ascorbic Acid, Retinyl Palmitate, Cholecalciferol, Fragrance, Methylparaben, Propylparaben, Diazolidinyl Urea, Disodium EDTA, Cymbopogon Flexuosus (Lemongrass) Oil,

  • PRINCIPAL DISPLAY PANEL

    Label

  • INGREDIENTS AND APPEARANCE
    DEEP COVER BUG BITE RELIEF 
    benzocaine ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84806-147
    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
    LEMONGRASS OIL (UNII: 5BIA40E9ED)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    PEG-2 STEARATE (UNII: 94YQ11Y95F)  
    CLOVE OIL (UNII: 578389D6D0)  
    MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    WATER (UNII: 059QF0KO0R)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84806-147-0399 g in 1 JAR; Type 0: Not a Combination Product07/24/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01707/24/2024
    Labeler - Morrisons Outdoors, LLC (031317468)
    Registrant - Derma Care Research Labs, LLC (116817470)
    Establishment
    NameAddressID/FEIBusiness Operations
    Derma Care Research Labs, LLC116817470manufacture(84806-147)
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