Label: EMUAID- silver ointment

  • NDC Code(s): 55926-0024-2
  • Packager: Speer Laboratories, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated January 14, 2021

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  • Active Ingredient

    Argentum Metallicum

    10x, 20x, 30 HPUS*

    * HPUS indicates that this ingredient is officially a part of the Homeopathic Pharmacopia of the United States

  • Purpose

    Topical Antiseptic, Analgesic, Anti-Inflammatory

  • Indications for Use

    For the relief of these symptoms due to minor wounds and burns, bruises, ulcerations, sunburn, razor burn, scrapes, rashes, blisters, bug bites, and skin eruptions from acne, eczema, or minor infection: • burning • stinging • itching • redness • stiffness • minor pain • minor inflammation

  • Warnings

    For external use only.  If skin condition persists after 7 days, or returns, consult a physician immediately.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • Directions

    Apply a thin layer of Emuaid over affected area, and repeat 3-4 times daily or as needed to relieve symptoms.

  • Other Ingredients

    Emu oil, Soybean Oil, Palm Oil, Canola Oil, Candelilla Wax, Lactobacillus Reuteri, Tribehenin, Glyceryl Behenate, Lysine Hydrochloride, Hydrogenated Castor Oil, Squalane, Tea Tree Oil, .Alpha.-Tocopherol Acetate, Phytosphingosine, Ceramide 3, Olive Oil, Allantoin, Silver Citrate

  • SPL UNCLASSIFIED SECTION

    Distributed by Speer Laboratories, LLC

    Pompano Beach, FL 33080

  • EumAidHomeopathic Medicine 

    First Aid Ointment

    Reduces pain, infection, and inflammation

    .1% Phytosphingosine

    2 fl oz/ 59 mL

    Emuaid092712

  • INGREDIENTS AND APPEARANCE
    EMUAID 
    silver ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55926-0024
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER10 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    Emu Oil (UNII: 344821WD61)  
    Soybean Oil (UNII: 241ATL177A)  
    Palm Oil (UNII: 5QUO05548Z)  
    Canola Oil (UNII: 331KBJ17RK)  
    CANDELILLA WAX (UNII: WL0328HX19)  
    Lactobacillus Reuteri (UNII: 9913I24QEE)  
    Tribehenin (UNII: 8OC9U7TQZ0)  
    GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)  
    Lysine Hydrochloride (UNII: JNJ23Q2COM)  
    Hydrogenated Castor Oil (UNII: ZF94AP8MEY)  
    Squalane (UNII: GW89575KF9)  
    Tea Tree Oil (UNII: VIF565UC2G)  
    .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
    Phytosphingosine (UNII: GIN46U9Q2Q)  
    Ceramide 3 (UNII: 4370DF050B)  
    Olive Oil (UNII: 6UYK2W1W1E)  
    Allantoin (UNII: 344S277G0Z)  
    Silver Citrate (UNII: CKA421A1J7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55926-0024-259 mL in 1 PACKAGE; Type 0: Not a Combination Product01/17/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/16/2014
    Labeler - Speer Laboratories, LLC (064900125)
    Establishment
    NameAddressID/FEIBusiness Operations
    Product by O2, Inc.136932444manufacture(55926-0024)
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