Label: TERRASIL S.O.S. FORMULA- natrum muriaticum, ranunculus bulbosus ointment

  • 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 May 13, 2014

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  • Active Ingredients

    Natrum Muriaticum 6X HPUS, Ranunculus Bulbosus 10X HPUS

    The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States

  • Purpose

    Natrum Muriaticum - Zoster Shingle Symptom Relief

    Ranunculus Bulbosus - Zoster Shingle Blisters, Stinging Pain

  • Uses

    Symptomatic treatment of shingles

  • Warnings

    For external use only.
    Virally based infections are contagious. This product will not stop the spread of viral infections.
    Do not use - in the eyes - over large areas of the body - if you are allergic to any ingredient in this product.
    Ask a doctor before use if pregnant or nursing.
    Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days.

    Keep out of reach of children.

    If swallowed, call poison control or seek medical help.

  • Directions

    Wash and dry affected skin. Apply a thin layer of Terrasil. Repeat procedure 2-3 times daily until symptoms are relieved. Store at room temperature.

  • Inactive Ingredients

    cera alba (organic beeswax), juniperus virginiana (cedarwood) oil, magnesium oxide, palmarosa oil, silver oxide, simmondsia chinensis (jojoba) seed oil, zinc oxide

  • PRINCIPAL DISPLAY PANEL - 44g Label

    terrasil ​with Activated Minerals

    S.O.S. Formula
    Fast. Soothing. All-Natural.

    Jar Label

  • INGREDIENTS AND APPEARANCE
    TERRASIL S.O.S. FORMULA 
    natrum muriaticum, ranunculus bulbosus ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24909-148
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB) (RANUNCULUS BULBOSUS - UNII:AEQ8NXJ0MB) RANUNCULUS BULBOSUS10 [hp_X]  in 1 g
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE6 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    JOJOBA OIL (UNII: 724GKU717M)  
    JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)  
    MAGNESIUM OXIDE (UNII: 3A3U0GI71G)  
    PALMAROSA OIL (UNII: 0J3G3O53ST)  
    SILVER OXIDE (UNII: 897WUN6G6T)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24909-148-1414 g in 1 JAR
    2NDC:24909-148-4444 g in 1 JAR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/13/2014
    Labeler - Aidance Skincare & Topical Solutions, LLC (018950611)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aidance Skincare & Topical Solutions, LLC018950611manufacture(24909-148) , label(24909-148)
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