FDA label 24b18e2a-0b89-0ae4-e063-6394a90a7116

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
93537cd1-074b-d6c3-e053-2a95a90a0b7e
SPL ID
24b18e2a-0b89-0ae4-e063-6394a90a7116
Version
2
Effective date
2024-10-17
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:32:47

Warnings cross-check#

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

Warnings sections page 1 of 1 · 3 matching rows.

warnings

For external use only. Ask a doctor before use is you have an overactive thyroid. Do not use if pregnant, nursing, or for long term use. Avoid use in eyes or eye area. If irritation occurs, stop use. Ask a doctor if condition worsens, symptoms last more than 7 days or clear up and occur again within a few days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

warnings

Avoid use in eyes or eye area. If irritation occurs, stop use.

warnings

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.