FDA label ec598568-951a-036b-e053-2a95a90a38a9

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
a648ae21-cbb0-41eb-8741-7b92d69f7973
SPL ID
ec598568-951a-036b-e053-2a95a90a38a9
Version
3
Effective date
2022-10-31
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:59:41

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 THIS PRODUCT IS NOT EFFECTIVE ON THE SCALP OR NAILS DO NOT USE IF SEAL IS BROKEN OR IS NOT VISIBLE WHEN USING WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES OR MOUTH STOP USE AND ASK A DOCTOR STOP USE AND ASK A PHYSICIAN IF IRRITATION OCCURS CHILDREN SUPERVISE CHILDREN IN THE USE OF THIS PRODUCT STORE UNDER STORE UNDER 30C (86F)

Reported adverse events (FAERS/openFDA)#

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