ZymaDerm

Manufacturer
Naturopathix, Inc.
Effective date
2021-01-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:14:07

Label at a glance#

ProductZymaDerm
Active ingredientSILVER NITRATE, ECHINACEA ANGUSTIFOLIA, FUCUS VESICULOSUS, THUJA OCCIDENTALIS LEAFY TWIG
Label structure8 sections

Indications and uses

Helpful as an aid in the treatment of molluscum contagiosum warts

Dosage and administration

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.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

ZymaDerm® for Molluscum - Drug Facts

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

5x Argentum nitricum HPUS 10%

7x Echinacea agustifolia HPUS 10%

7x Fucus vesiculosus HPUS 10%      

7x Thuja occidentalis HPUS 10%      

Purpose:

OTC - PURPOSE SECTION

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:

INDICATIONS & USAGE SECTION

Helpful as an aid in the treatment of molluscum contagiosum warts

Warnings:

WARNINGS SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation, itching, redness of the skin develop.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions:

DOSAGE & ADMINISTRATION SECTION

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:

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 69163-4136-1
ZymaDerm
FOR MOLLUSCUM
Homeopathic

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69163-4136-12023-01-30C16284748780-1f386c649-e7c5-0266-e053-dadaa90a7c1aZymaderma For Molluscum

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69163-4136-1ZymaDerm1 in 1 BOXLIQUID13
69163-4136-1ZymaDerm13 mL in 1 BOTTLE, GLASSLIQUID133

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69163-4136ZYMADERM (SILVER NITRATE, ECHINACEA ANGUSTIFOLIA, FUCUS VESICULOSUS AND THUJA OCCIDENTALIS LEAFY TWIG) LIQUID [NATUROPATHIX, INC.]3Legacy NDC, 2 package rows20210113_790b82ad-c19a-4278-bef2-c7e7244ca390.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69163-413669163-4136-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4cd4a979-4943-4f65-9d19-abfb5952ce2f790b82ad-c19a-4278-bef2-c7e7244ca3902021-01-15WarningsExact identifier
spl id: 4cd4a979-4943-4f65-9d19-abfb5952ce2f
spl set id: 790b82ad-c19a-4278-bef2-c7e7244ca390

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.