FDA label 38619d96-814e-71ee-e063-6294a90af33e

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)

SPL set ID
38619d96-814d-71ee-e063-6294a90af33e
SPL ID
38619d96-814e-71ee-e063-6294a90af33e
Version
1
Effective date
2025-06-25
Source export date
2026-11-06
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/3744b3ae389d13e8f30cade845ea29e0fc75bb043dcda980c2025693f0c10522/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 09:08:27

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

1.Do not use if the head skin isinjured. damaged or infected. 2.Avoid contact with eyes. lf it ent-erseyes accidentally, please washit withwater immediately. 3.Discontinue use if discomfort occurs. 4.This product should be stored inacool, dark place. 5.Not for use by children or preg-nant/nursing women.

Reported adverse events (FAERS/openFDA)#

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