FDA.reportPublic FDA data

FDA label 0f487b86-c3a7-0b63-e063-6294a90a87fa

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
0f487b86-c3a6-0b63-e063-6294a90a87fa
SPL ID
0f487b86-c3a7-0b63-e063-6294a90a87fa
Version
1
Effective date
2024-01-19
Source export date
2026-09-28
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/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:37:38

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 . This product is for external use. lt is forbidden to take orally. 2. It is forbidden for pregnant women and those who are allergic to this product, and should be used with caution for those with allergic constitution. 3. lt is forbidden to paste on the skin with ulceration, damage and infection. 4. For foreign bodies in the external auditory canal, you should go to the hospital. 5. Children must use it under the supervision of adults. 6. This product is a health care product and cannot replace drugs and medical devices.

Reported adverse events (FAERS/openFDA)#

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