FDA label 347f922b-089c-23b9-e063-6394a90a3c7c

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
347f922b-089b-23b9-e063-6394a90a3c7c
SPL ID
347f922b-089c-23b9-e063-6394a90a3c7c
Version
1
Effective date
2025-05-20
Source export date
2026-10-12
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/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:26:39

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

For external use only. Do not use: On irritated skin or any area that is infected or reddened If allergic to any of the ingredients. If pregnant or breastfeeding, unless directed by a doctor. Avoid contact with eyes Stop use and ask a doctor if: discomfort, burning, or irritation occurs lf no improvement within 4 weeks Do not use: If pregnant or breastfeeding, unless directed by a doctor. Keep out of reach of children. If product gets intoeyes,flush with water for 15 minutes. If swallowed, get medical help or contact a Poison Control Center immediately

Reported adverse events (FAERS/openFDA)#

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