FDA label 6507bf97-6250-234b-e053-2991aa0a2d18

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
3773fe01-2206-206c-e054-00144ff88e88
SPL ID
6507bf97-6250-234b-e053-2991aa0a2d18
Version
4
Effective date
2018-02-12
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 05:12:47

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. Back panel When using this product do not get into eyes Stop use and ask a physician if Allergic reaction occurs Condition worsens or does not improve within 7 days Symptoms clear up and return within a few days Redness, irritation, swelling, pain or other symptoms begin or increase Do not Use in or near the eyes Use in large quantities, particularly over raw surfaces or blistered areas Keep out of reach of children If swallowed get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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