FDA.reportPublic FDA data

Derman Antifungal

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Derman Antifungal
Generic name
ZINC UNDECYLENATE
Manufacturer
Compania Internacional de Comercio, S.A.P.I de C.V.
Product type
HUMAN OTC DRUG
SPL set ID
0129d801-90f6-49fd-857f-27d6ba9fc66c
SPL ID
43fa85f0-78bd-9e8d-e063-6294a90ab9da
Version
24
Effective date
2025-11-19
Source export date
2026-08-01
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/054d07cb7b0dcd436e53c5bdecbb921b48860de8ff372c4a586941aa9821a276/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:23:08
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use on children under 2 years of age, unless directed by a doctor. When using this product Avoid contact with the eyes. Stop use and ask a doctor if irritation occurs or if there is no improvement within 4 weeks. Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.