FDA label 3f01a409-a521-bddc-e063-6394a90a3011

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
d825893d-e902-75d9-e053-2a95a90a477f
SPL ID
3f01a409-a521-bddc-e063-6394a90a3011
Version
2
Effective date
2025-09-17
Source export date
2026-10-30
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/2026-10-30/023bc8d8aae5addb7530087bbbdb169b3ccbf36764f15b8ca67db07e1e5aea8b/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:11:41

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 external use only Keep out of reach of children Stop use and ask a doctor • if you experience worsening symptoms or if symptoms last longer than 7 days • Avoid contact with the eyes or mucous membranes • Do not apply to wounds or damaged skin • Wash hands after use If pregnant or breastfeeding, • ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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