FDA.reportPublic FDA data

FDA label 2a83dd52-3a8e-cf92-e063-6394a90a4605

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
9800cae0-d58b-4890-8fe9-97f0ced63faa
SPL ID
2a83dd52-3a8e-cf92-e063-6394a90a4605
Version
4
Effective date
2024-12-30
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:04:25

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings USE ONLY AFTER DIAGNOSIS BY A PHYSICIAN AND UNDER THE SUPERVISION OF A PHYSICIAN. For External Use Only. Children under 2 years of age should be seen by a physician. Initial worsening of symptoms may occur. Physician should always be consulted to rule out serious conditions.

warnings

Contact lens wearers consult physician prior to using. To avoid contamination - do not touch tip to any surface. Replace cap after every use. Use within 30 days of opening. EXPIRATION DATE ONLY REFERS TO THE UNOPENED BOTTLE. The use of this container by more than one person may spread infection.

Reported adverse events (FAERS/openFDA)#

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