FDA label 2cdf6fb1-2ad9-5d35-e063-6394a90adb80

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
afbc5747-460a-405d-b102-9ee1a581b11b
SPL ID
2cdf6fb1-2ad9-5d35-e063-6394a90adb80
Version
5
Effective date
2025-01-29
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:04:33

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. Do not use: • in the eyes • over large areas of the body • if you are allergic to any of the ingredients. Ask a doctor before use if you have • deep or puncture wounds • animal bites • serious burns. Stop use and ask a doctor if • you need to use longer than 1 week • condition persists or gets worse • symptoms persist for more than 1 week, or clear up and reoccur • rash or other allergic reaction develops. Keep out of reach of children. • Do not use if pregnant or breastfeeding

Reported adverse events (FAERS/openFDA)#

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