Label: ZYMADERM- silver nitrate, echinacea angustifolia, fucus vesiculosus and thuja occidentalis leafy twig liquid

  • 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 15, 2021

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  • SPL UNCLASSIFIED SECTION

    ZymaDerm® for Molluscum - Drug Facts

  • Active Ingredients:

    5x Argentum nitricum HPUS 10%

    7x Echinacea agustifolia HPUS 10%

    7x Fucus vesiculosus HPUS 10%      

    7x Thuja occidentalis HPUS 10%      

  • Purpose:

    Topical antiseptic

    Anti-inflammatory

    Topical antiseptic

    Wart treatment

    The letters ‘HPUS’ indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States

  • Uses:

    Helpful as an aid in the treatment of molluscum contagiosum warts

  • Warnings:

    Ask a doctor before use if you are allergic to iodine. Contains seaweed, which contains iodine.

    Stop use and ask a doctor

    if irritation, itching, redness of the skin develop.

    Keep out of reach of children.

  • Directions:

    For external use only. Apply directly to each molluscum bump twice a day using the applicator rod attached to the cap. Continue for 3-4 weeks, or as long as needed. More details inside package.

  • Other Ingredients:

    Essential oil of M. alternifolia and B. citriodora, high selenium canola oil, clove oil, fractionated coconut oil.

    The FDA has not evaluated this product or these claims. ZymaDerm™ is not intended to diagnose, treat, cure or prevent any disease.

  • PRINCIPAL DISPLAY PANEL

    NDC 69163-4136-1
    ZymaDerm
    FOR MOLLUSCUM
    Homeopathic

    PRINCIPAL DISPLAY PANEL NDC 69163-4136-1 ZymaDerm FOR MOLLUSCUM Homeopathic

  • INGREDIENTS AND APPEARANCE
    ZYMADERM 
    silver nitrate, echinacea angustifolia, fucus vesiculosus and thuja occidentalis leafy twig liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69163-4136
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE5 [hp_X]  in 13 mL
    ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA7 [hp_C]  in 13 mL
    FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS7 [hp_X]  in 13 mL
    THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG7 [hp_X]  in 13 mL
    Inactive Ingredients
    Ingredient NameStrength
    TEA TREE OIL (UNII: VIF565UC2G)  
    BACKHOUSIA CITRIODORA WHOLE (UNII: 2P8IL6SP2R)  
    CANOLA OIL (UNII: 331KBJ17RK)  
    CLOVE OIL (UNII: 578389D6D0)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69163-4136-11 in 1 BOX04/22/2013
    113 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED HOMEOPATHIC04/22/2013
    Labeler - Naturopathix, Inc. (788743362)
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