Label: ZYMADERM FOR SHINGLES- melissa officinalis, argentum nitricum, echinacea angustifolia, fucus vesiculosus liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69163-4137-1 - Packager: Naturopathix, Inc.
- 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
If you are a consumer or patient please visit this version.
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- SPL UNCLASSIFIED SECTION
- Purpose:
- Uses:
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Directions:
- Use the applicator rod to apply a thin layer to the affected skin.
- Apply every 2 hours if possible, but at least 4 times a day.
- Begin use at the earliest sign of prodromal symptoms to help abort actual outbreaks.
- ZymaDerm™ should be applied to the blisters directly, minimizing contact with normal skin. Spills on skin should be washed with soap and water; eyes should be flushed with water in case of accidental contact; Apply enough to cover the blisters; more is not better!
- Continue use until the blisters dry up, or until the prodromal symptoms (burning, tingling, itching, pain) are gone.
- As long as you do not experience intense, persistent itchiness or discomfort, you may continue application.
- Use the applicator rod to apply a thin layer to the affected skin.
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Warnings:
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For External use only – ZymaDerm® contains iodine.
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ZYMADERM® IS NOT TO BE TAKEN INTERNALLY. However it may be used safely on the skin, lips, and mucosal surfaces.
- If you are pregnant, allergic to iodine, tea tree oil or any of the ingredients, consult your physician prior to use.
- Accidental contact – Eyes should be flushed with water. Ingestion: in the case of accidental ingestion, drink water and then seek medical attention. Spills on counter surfaces may be cleaned with rubbing alcohol.
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For External use only – ZymaDerm® contains iodine.
- Active Ingredients
- Purpose
- Other Ingredients:
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ZYMADERM FOR SHINGLES
melissa officinalis, argentum nitricum, echinacea angustifolia, fucus vesiculosus liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69163-4137 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MELISSA OFFICINALIS (UNII: YF70189L0N) (MELISSA OFFICINALIS - UNII:YF70189L0N) MELISSA OFFICINALIS 3 [hp_X] in 13 mL SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 5 [hp_X] in 13 mL ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA 5 [hp_X] in 13 mL FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS 7 [hp_X] in 13 mL Inactive Ingredients Ingredient Name Strength JOJOBA OIL (UNII: 724GKU717M) CANOLA OIL (UNII: 331KBJ17RK) PEPPERMINT OIL (UNII: AV092KU4JH) WEST INDIAN LEMONGRASS OIL (UNII: 5BIA40E9ED) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69163-4137-1 1 in 1 BOX 01/01/2020 1 13 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 01/01/2020 Labeler - Naturopathix, Inc. (788743362)