Label: PAIN RELIEF ROLL ON- topical analgesic liquid

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

Drug Label Information

Updated April 15, 2024

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  • Active Ingredient

    Menthol 6%

    Camphor 5%

    Capsaicin 0.025%

  • Purpose

    Topical Analgesic

  • Uses:

    For the temporary relief of aches and pains of muscles and joints associated with arthritis, backaches, strains or sprains

  • Warnings

    For External use only

  • When using this product

    Use only as directed. Avoid contact with eyes or mucous membranes. Do not apply directly to wounds or damaged skin. Do not use in combination with other ointments, creams, or sprays. Wash hand with cool water after each uyse. Do not use with a heating pad or device.

  • Stop usage immediately and ask a doctor if:

    Condition worsens or symptoms persist for more than 7 days

  • If pregnant or breast-feeding:

    Ask a health professional before use

  • Keep out of reach of children:

    If ingested get medical help or contact Poison control center immediately: 1-800-222-1222

  • Directions:

    Adults and Children over 12 years old: Apply to afected area - do not apply more than 4 times daily. Children 12 years or younger: consult a doctor

  • Inactive Ingredients

    Citrus Fiber, Dimethicone, Isopropyl Alcohol, Jojoba Oil, Phenoxyethanol, Simethicone, Water

  • Insta Eaze: Roll the Pain Away

    Insta Eaze Roll the Pain Away

  • INGREDIENTS AND APPEARANCE
    PAIN RELIEF ROLL ON 
    topical analgesic liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79804-282
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.06 g  in 1 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)0.05 g  in 1 g
    CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN0.00025 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    JOJOBA OIL (UNII: 724GKU717M)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CITRUS FRUIT (UNII: XDK00Z8012)  
    Product Characteristics
    Colorwhite (Semi-Translucent) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79804-282-0387 g in 1 PACKAGE; Type 0: Not a Combination Product11/07/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/07/2022
    Labeler - Eagle Labs Inc (118496872)
    Registrant - Eagle Labs Inc (118496872)
    Establishment
    NameAddressID/FEIBusiness Operations
    Eagle Labs Inc118496872manufacture(79804-282) , pack(79804-282) , label(79804-282)
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