FDA label 331e31c7-15f4-4b0a-8a1a-e1af46ca284c

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
cff85b40-9d3f-4535-a306-6d72e3948ddd
SPL ID
331e31c7-15f4-4b0a-8a1a-e1af46ca284c
Version
2
Effective date
2013-08-15
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 05:13:37

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. Initial exacerbation of symptoms may occur. Use only if single-use dropper is intact. To avoid contamination, do not touch the tip of the dropper to any surface. Do not reuse. Once opened, discard. Contact wearers: consult a physician prior to using. Do not use: if solution changes color or becomes cloudy Stop use and ask a doctor if: symptoms worsen or persist for more than 72 hours changes in vision occur you experience eye pain If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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