Label: PAIN AWAY- analgesic spray

  • NDC Code(s): 79804-265-04, 79804-265-08
  • Packager: Eagle Labs Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 15, 2024

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  • ACTIVE INGREDIENT

    Capsacin; Analgesic

    Menthol: Analgesic

    Camphor: Analgesic

  • PAIN RELIEF - TOPICAL ANALGESIC

    Analgesic

  • Indications

    For the temporary relief of minor aches and pains of muscles and joints associated with

    Simple backache
    Arthritis
    Strains
    Bruises
    Sprains

  • Warnings

    • For extrernal use only
    • Avoid Contact with the eyes
    • Do not apply to wounds or bandaged skin
    • Do not bandage tightly

    Stop use and consult a doctor if:

    • Condition worsens
    • Symptoms persist for more than 7 days or cleear up and reoccur
    • Redness is present
    • irritation develops

    When using this product

    • Use only as directed
    • Do not apply heat (heating pads) or apply patches to area

    Keep out of children

    If accidentally swallowed get medical help or contact a poison control center immediately

    If pregnant or breastfeeding

    If pregnant or breastfeeding, ask a health professional before use.

    Keep out of the reach o children

    If accidentally swallowed get medical help or contact a poison control center immediately

    Flammable

    Keep away from excessive heat or open flame

    Flammable

    Keep away from excessive heat or open flame

  • Inactive Ingredients

    Isopropanol, MCT, Phenoxyethanol, Simethicone

  • Directions

    Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age consult a doctor.

  • Pain Relief Pro

    Pain Relief Pro

  • Insta Eaze Spray the Pain Away

    Insta Eaze Spray the Pain Away

  • INGREDIENTS AND APPEARANCE
    PAIN AWAY 
    analgesic spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79804-265
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.16 g  in 1 g
    CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN0.001 g  in 1 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)0.11 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PALM OIL (UNII: 5QUO05548Z)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79804-265-04108 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2022
    2NDC:79804-265-08216 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01707/01/2022
    Labeler - Eagle Labs Inc. (118496872)
    Registrant - Eagle Labs Inc (118496872)
    Establishment
    NameAddressID/FEIBusiness Operations
    Eagle Labs Inc118496872manufacture(79804-265) , label(79804-265) , pack(79804-265)
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