FDA label 5264f800-165f-4c28-e063-6394a90a0e1b

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
3b0d79ad-7d84-5f69-e063-6294a90a5a36
SPL ID
5264f800-165f-4c28-e063-6394a90a0e1b
Version
2
Effective date
2026-05-22
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:39:13

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 Always perform a 24-hour patch test prior to use; discontinue if irritation occurs, avoid application on broken skin or if allergic to nuts, seeds, or essential oils (e.g., almond, tea tree, lavender), and consult a healthcare provider before use during pregnancy, breastfeeding, or for children under 12.

Reported adverse events (FAERS/openFDA)#

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