FDA label 58357e6f-2d43-456f-ae1f-91794ce8f402

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
e889739a-a85b-47ed-b44d-e5a30be0f45b
SPL ID
58357e6f-2d43-456f-ae1f-91794ce8f402
Version
2
Effective date
2024-10-09
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:29:43

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: ​For exteral use only. 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. ​When using this product ​ -Do not get into eyes - Do not apply to broken or abraded skin. ​Stop use and ask a doctor if ​ - Condition worsens - Symptoms last more than 7 days.

Reported adverse events (FAERS/openFDA)#

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