FDA label 10f40497-0a40-0e47-e063-6294a90a2b62

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
7e2b3838-3e79-4256-91ea-70365f1acb25
SPL ID
10f40497-0a40-0e47-e063-6294a90a2b62
Version
3
Effective date
2024-02-09
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 02:26:48

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 Flammable, keep away from fire and flame Does not contain grain alcohol; do not drink if taken internally will produce serious gastric distric disturbances. When using this product Avoid the eyes and mucous membranes In the case of eyes or mucous membranes contact, rinse area thoroughly with water Stop use and ask a doctor if Condition worsens Redness or irritation develops Condition persists for more than 3 days Keep out of reach of children If swallowed,contact a doctor or Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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