FDA label 43d2bef5-bf18-b63d-e063-6294a90a84fb

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
c54b3986-2dc1-b42e-e053-2995a90a274b
SPL ID
43d2bef5-bf18-b63d-e063-6294a90a84fb
Version
7
Effective date
2025-11-17
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:57:20

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 Warnings: A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES. For External Use Only. • This product is intended to complement, not replace, standard medical treatment. • Initial worsening of symptoms may occur. 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.