Home NDC 69163-4136-1 ZymaDerm
Product NDC 69163-4136
Requested package NDC 69163-4136-1
11-digit product format 691634136
Labeler code 69163
Product ID 69163-4136_4cd4a979-4943-4f65-9d19-abfb5952ce2f
Type HUMAN OTC DRUG
Nonproprietary name SILVER NITRATE, ECHINACEA ANGUSTIFOLIA, FUCUS VESICULOSUS and THUJA OCCIDENTALIS LEAFY TWIG
Dosage form LIQUID
Route TOPICAL
Labeler Naturopathix, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2013-04-22
Marketing end 0000-00-00
Substance SILVER NITRATE; ECHINACEA ANGUSTIFOLIA; FUCUS VESICULOSUS; THUJA OCCIDENTALIS LEAFY TWIG
Active strength 5 [hp_X]/13mL; [hp_C]/13mL; [hp_X]/13mL; [hp_X]/13mL
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record
Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69163-4136-1 ZymaDerm 1 in 1 BOX LIQUID 1 3 69163-4136-1 ZymaDerm 13 mL in 1 BOTTLE, GLASS LIQUID 13 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69163-4136 ZYMADERM (SILVER NITRATE, ECHINACEA ANGUSTIFOLIA, FUCUS VESICULOSUS AND THUJA OCCIDENTALIS LEAFY TWIG) LIQUID [NATUROPATHIX, INC.] 3 Legacy NDC, 2 package rows 20210113_790b82ad-c19a-4278-bef2-c7e7244ca390.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 69163-4136-1 69163413601 1 BOTTLE, GLASS in 1 BOX (69163-4136-1) > 13 mL in 1 BOTTLE, GLASS 2013-04-22 0000-00-00 No No Current