Label: WARRIOR CHIGGEREX RELIEF- benzocaine 10% cream

  • NDC Code(s): 72839-069-01
  • Packager: Derma Care Research Labs, LLC
  • 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 April 18, 2022

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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

    Ascorbic Acid, Aloe Barbadensis Leaf Extract, Camphor, Chamomilla Recutita (Matricaria) Flower Extract, Cholecalciferol, Diazolidinyl Urea, Disodium EDTA, Eugenia Caryophyllus (Clove) Flower Oil, Fragrance, Mentha Piperita (Peppermint) Oil, Methylparaben, Octyldodecanol, Olea Europaea (Olive) Fruit Extract, PEG-2 Stearate, PEG-2 Stearate SE, PEG-8 Dimethicone, Propylene Glycol, Propylparaben, Pyridoxine HCl, Retinyl Palmitate, Silica, Sodium Propoxyhydroxypropyl Thiosulfate Silica, Tocopheryl Acetate, Water, Zea Mays (Corn) Oil.

  • PRINCIPAL DISPLAY PANEL

    Label

  • INGREDIENTS AND APPEARANCE
    WARRIOR CHIGGEREX RELIEF 
    benzocaine 10% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72839-069
    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
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    PEG-2 STEARATE (UNII: 94YQ11Y95F)  
    CLOVE OIL (UNII: 578389D6D0)  
    MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    4-DESOXYPYRIDOXINE HYDROCHLORIDE (UNII: P9QAN95HHX)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    CORN OIL (UNII: 8470G57WFM)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    WATER (UNII: 059QF0KO0R)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72839-069-0150 g in 1 JAR; Type 0: Not a Combination Product08/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34808/14/2020
    Labeler - Derma Care Research Labs, LLC (116817470)
    Registrant - Derma Care Research Labs, LLC (116817470)
    Establishment
    NameAddressID/FEIBusiness Operations
    Derma Care Research Labs, LLC116817470manufacture(72839-069)
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