Label: MAXIMUM STRENGTH BLUE EMU PAIN RELIEF BLU EMU- trolamine salicylate spray

  • NDC Code(s): 69993-100-04
  • Packager: Kingsway Pharmaceuticals dba NFI, LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated January 31, 2025

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  • Active ingredient

    Trolamine salicylate 10%

  • Purpose

    Topical analgesic

  • Uses

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

    •
    simple backache
    •
    arthritis
    •
    strains
    •
    bruises and sprains
  • Warnings

    For external use only

    Allergy alert:

    If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

    When using this product

    •
    use only as directed
    •
    do not bandage tightly or use with a heating pad
    •
    avoid contact with eyes or mucous membranes
    •
    do not apply to wounds or damaged skin.

    Stop use and ask a doctor if

    •
    condition worsens
    •
    symptoms persist for more than 7 days or clear up and occur again within a few days
    •
    redness is present
    •
    irritation develops.

    If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    adults and children over 12 years:

    •
    apply generously to affected area
    •
    massage into painful area until thoroughly absorbed into skin
    •
    repeat as necessary, but no more than 4 times daily

    children 12 years or younger: ask a doctor.

  • Inactive ingredients

    Aloe Barbadensis Leaf Juice, Caprylyl Glycol, CI 77491, Dimethyl Sulfone, Disodium EDTA, Emu Oil, Ethylhexylglycerin, Glucosamine Sulfate Potassium Chloride, Glycerin, Glyceryl Caprylate, Lecithin, Oleic Acid, Panthenol, Phenoxyethanol, Polysorbate 20, Sorbitol, Water, Xanthan Gum.
     

  • SPL UNCLASSIFIED SECTION

    TOLL FREE: 1-800-432-9334
    WWW.BLUE-EMU.COM
    MANUFACTURED IN THE USA
     
    KINGSWAY™
    PHARMACEUTICALS 
     
    Distributed By: Kingsway Pharmaceuticals
    dba NFI Consumer Products
    636 SHELBY STREET STE. 300
    BRISTOL, TN 37620

  • PRINCIPAL DISPLAY PANEL - Can Label

    ANY DIRECTION PAIN
    RELIEF SPRAY
     
    Arthritis,
    Muscles
    & Joints
     
    BLUE-EMU®
     
    Continuous
    Spray
     
    Twist-N-Lock
    TOP
    360º Spray
     
    AMERICA'S
    #1
    EMU OIL FORMULA
    ODOR
    FREE
     
    Contains Emu Oil
    Topical Analgesic Spray
    4.0 oz Net Wt. (113g)
     
    image-01

  • INGREDIENTS AND APPEARANCE
    MAXIMUM STRENGTH BLUE EMU PAIN RELIEF  BLU EMU
    trolamine salicylate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69993-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Trolamine Salicylate (UNII: H8O4040BHD) (Salicylic Acid - UNII:O414PZ4LPZ) Trolamine Salicylate10 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    EMU OIL (UNII: 344821WD61)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLUCOSAMINE SULFATE POTASSIUM CHLORIDE (UNII: 15VQ11I66N)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)  
    SOYBEAN LECITHIN (UNII: 1DI56QDM62)  
    OLEIC ACID (UNII: 2UMI9U37CP)  
    Panthenol (UNII: WV9CM0O67Z)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Polysorbate 20 (UNII: 7T1F30V5YH)  
    SORBITOL (UNII: 506T60A25R)  
    Water (UNII: 059QF0KO0R)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69993-100-04118 mL in 1 CAN; Type 0: Not a Combination Product06/04/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01706/04/2012
    Labeler - Kingsway Pharmaceuticals dba NFI, LLC (121681919)
    Registrant - Kingsway Pharmaceuticals dba NFI, LLC (121681919)
    Establishment
    NameAddressID/FEIBusiness Operations
    Formulated Solutions, LLC143266687MANUFACTURE(69993-100)
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