FDA label 95c10c24-b5ca-864d-e053-2995a90a3235

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
49b12d66-26c6-263d-e054-00144ff88e88
SPL ID
95c10c24-b5ca-864d-e053-2995a90a3235
Version
3
Effective date
2019-10-25
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:21:53

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 esternal use only. Avoid contact with the eyes. Do not bandage tightly or use hearing pad. Do not apply to open wounds or damaged skin. Discontinue use of this product and consult a physician if condition worsens, symptons persist for more than 7 days, or excessive skin irrirtation occurs.

Reported adverse events (FAERS/openFDA)#

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