NDC 69163-4131

ZymaDerm

Iodine, Thuja Occidentalis Whole And Echinacea, Unspecified

ZymaDerm is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Naturopathix, Inc.. The primary component is Iodine; Thuja Occidentalis Whole; Echinacea, Unspecified.

• Product ID: 69163-4131_8b24a2cb-c95f-411c-aeb7-6305b85e6ee7
• NDC: 69163-4131
• Product Type: Human Otc Drug
• Proprietary Name: ZymaDerm
• Generic Name: Iodine, Thuja Occidentalis Whole And Echinacea, Unspecified
• Dosage Form: Liquid
• Route of Administration: TOPICAL
• Marketing Start Date: 2013-04-22
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Naturopathix, Inc.
• Substance Name: IODINE; THUJA OCCIDENTALIS WHOLE; ECHINACEA, UNSPECIFIED
• Active Ingredient Strength: 5 [hp_X]/13mL; [hp_C]/13mL; [hp_C]/13mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 69163-4131-1

1 BOTTLE, GLASS in 1 BOX (69163-4131-1) > 13 mL in 1 BOTTLE, GLASS

• Marketing Start Date: 2013-04-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69163-4131-1 [69163413101]

ZymaDerm LIQUID

• Marketing Category: UNAPPROVED HOMEOPATHIC
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-04-22
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
IODINE	5 [hp_X]/13mL

OpenFDA Data

• SPL SET ID: 4924433f-4250-4dbf-b85f-16255ceb1641
• Manufacturer:
  • Naturopathix, Inc.
• UNII:
  • 5HBV6WCE3N
  • 4N9P6CC1DX
  • 9679TC07X4
• UPC Code:
  • 0898407001016

NDC Crossover Matching brand name "ZymaDerm" or generic name "Iodine, Thuja Occidentalis Whole And Echinacea, Unspecified"

NDC	Brand Name	Generic Name
69163-4131	ZymaDerm	Iodine, Thuja Occidentalis Whole and Echinacea, Unspecified
69163-4136	ZymaDerm	SILVER NITRATE, ECHINACEA ANGUSTIFOLIA, FUCUS VESICULOSUS and THUJA OCCIDENTALIS LEAFY TWIG