FDA label 71b2e6b1-a1df-5585-e053-2a95a90a7d3e

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
9be3ea70-3b20-4a5f-8732-17e5a4f11543
SPL ID
71b2e6b1-a1df-5585-e053-2a95a90a7d3e
Version
3
Effective date
2018-04-27
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:22:40

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. Avoid contact with eyes. Do not apply to open wounds or damaged skin. If you are taking any prescription medication or have any serious medical condition, ask a physician before use. If condition worsens, symptoms persist for more than 7 days, or rash or allergic reaction develops, stop use and ask a physician. If pregnant or nursing, ask a healthcare professional before use. Keep out of the reach of children. Do not use if tamper-resistant seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

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