FDA.reportPublic FDA data

FDA label a750d31c-6546-752a-e053-2a95a90a6e4d

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
a750a772-c091-4266-e053-2a95a90aa1d0
SPL ID
a750d31c-6546-752a-e053-2a95a90a6e4d
Version
1
Effective date
2020-06-05
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:19

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 1. For external use only. Flammable. Keep away fromheat or flame 2. This product is for external use, it is not allowed tobe taken orally, if it enters the eyes accidentallyplease wash it with water 3. Do not use if you are allergic to alcohol, if imitationor swelling occurs, please stop using, if it lasts formore than 72 hours, please consult doctor. 4. The product should be kept out of the reach of children5. The storage place of this product shall be dry, cleannormal temperature without sun exposure

Reported adverse events (FAERS/openFDA)#

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