FDA label 4bc8f090-0b96-4d07-bbde-b4d46fc71d3e

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
69bca4e5-5f67-4b22-9c26-00e9f5738d76
SPL ID
4bc8f090-0b96-4d07-bbde-b4d46fc71d3e
Version
3
Effective date
2014-06-06
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:12:58

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

Avoid application to wounded or infected area. Do NOT use if irritation develops. If so, consult a physician immediately. Keep out of reach of children. Cover lid after each use. Store at a cool, dry place, away from direct sunlight. Instantly rinse with cold water when product comes in contact with eye(s).

Reported adverse events (FAERS/openFDA)#

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