FDA label b7b34eb1-0b15-f7cf-e053-2995a90a3cbc

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
b7b34ea0-f38e-adbc-e053-2a95a90a4ea6
SPL ID
b7b34eb1-0b15-f7cf-e053-2995a90a3cbc
Version
1
Effective date
2020-12-30
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 02:24:09

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 or flame. Do not use in children less than 2 months of age on open skin wounds When using this product, keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor. Keep out of reach of children. If swallowed get medical help or call a poison control center immediately.

Reported adverse events (FAERS/openFDA)#

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