FDA label 32cc8fd5-7a5f-4db5-b4c1-063fc43946c4

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
5161800b-e0a7-489f-8268-42c053b6e1b0
SPL ID
32cc8fd5-7a5f-4db5-b4c1-063fc43946c4
Version
1
Effective date
2019-02-20
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 03:04:58

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 Warnings: 1. For external use only 2. Seek medical attention if rash, inflammation, itchiness or other symptoms appear during use of the product or after exposure to direct sunlight. 3. Do not use on open wounds 4. Storage and handling precaution 1) Keep out of reach of children 2) Store away from direct sunlight 5. Rinse your eyes with water if they are exposed to the product. 6. Product may cause hair loss or discoloration if not rinsed out thoroughly. 7. Product is slippery. Clean it immediately if dropped on floor.

Reported adverse events (FAERS/openFDA)#

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