FDA label 43d192ea-8283-3915-e063-6394a90a8095

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
e5bd53c1-8174-7b0c-e053-2995a90ac115
SPL ID
43d192ea-8283-3915-e063-6394a90a8095
Version
4
Effective date
2025-11-17
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:16:43

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: 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. • If pregnant or breast-feeding, ask a health professional before use. Contact lens wearers: Consult a physician before use. • Keep out of reach of children. • In case of accidental ingestion, get medical help or contact a Poison Control Center right away. • To avoid contamination – do not touch tip to any surface. • Replace cap after every use. • Use within 90 days of opening. • EXPIRATION DATE ONLY REFERS TO 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.