Label: HERPA ONE- natrum muriaticum,graphites,thuja ointment

  • NDC Code(s): 24909-220-01
  • Packager: Aidance Skincare & Topical Solutions, 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 12, 2023

If you are a consumer or patient please visit this version.

  • Active Ingredients and Purpose

    Natrum Muriaticum 6X HPUS - Genital Sores Relief

    Graphites 10 X HPUS - Itchy Lesion Relief

    Thuja 6X HPUS - Skin Eruptions, Itching or Burning Pain Relief.

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

  • Uses

    Relief of symptoms of genital sores

  • Warnings

    For external use only. This product is not a substitute for professional healthcare. Virally based infections are contagious.

    This product will not stop the spread of the virus that causes Herpes or other viruses.

    Do not use • in the eyes • over large areas of the body • if you are allergic to any ingredients 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 seek medical help

  • Directions

    Apply 2 to 3 times daily for soothing relief.

  • Inactive Ingredients

    Beeswax, Coconut Oil, Eucalyptus Oil, Lemongrass Oil, Lysine,Magnesium Oxide, Peppermint Oil, Silver Stearate, Zinc Oxide.

  • Questions?

    401-432-7750 or www.aidance.com

  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    HERPA ONE 
    natrum muriaticum,graphites,thuja ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24909-220
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE6 [hp_X]  in 44 g
    GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE10 [hp_X]  in 44 g
    THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N) (THUJA OCCIDENTALIS WHOLE - UNII:5HBV6WCE3N) THUJA OCCIDENTALIS WHOLE6 [hp_X]  in 44 g
    Inactive Ingredients
    Ingredient NameStrength
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    WEST INDIAN LEMONGRASS OIL (UNII: 5BIA40E9ED)  
    MAGNESIUM OXIDE (UNII: 3A3U0GI71G)  
    LYSINE (UNII: K3Z4F929H6)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    SILVER STEARATE (UNII: 4H6PCL92ZN)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24909-220-0144 g in 1 JAR; Type 0: Not a Combination Product09/07/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/07/2012
    Labeler - Aidance Skincare & Topical Solutions, LLC (018950611)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aidance Skincare & Topical Solutions, LLC018950611manufacture(24909-220)