FDA.reportPublic FDA data

FDA label b8689948-7367-31bb-e053-2995a90a3a0f

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
4ec07b44-1212-42dc-8369-0d5722a6a631
SPL ID
b8689948-7367-31bb-e053-2995a90a3a0f
Version
1
Effective date
2021-01-08
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 02:22:56

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 . Not for use on open wounds. • If symptoms persist or worsen, discontinue use, seek medical attention. • Avoid contact with eyes. If product gets into eyes, flush with water, seek medical attention. • If rash, redness, irritation or itching occurs, discontinue use. • If pregnant or breastfeeding ask a health professional before use. • If swallowed, get medical help or contact a Poison Center. • Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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