FDA label a808a3da-1b11-4ca8-96a1-dce16675e52e

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
5cfbe140-aab0-4378-871f-0bedf0cef02e
SPL ID
a808a3da-1b11-4ca8-96a1-dce16675e52e
Version
1
Effective date
2010-08-24
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:35:16

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 Some individuals may be sensitive to essential oils. Begin with a small drop to determine if the product causes any increased redness or irritation and discontinue use if it irritates your skin. AS with all medicine, if you are pregnant or breast-feeding, ask a health professional before use. Keep out of the reach of children. If accidental ingestion of more than several drops occurs, get medical help or contact a Poison Control Center. For external use only. Do not apply to the eyes or mucous membranes. Keep all medicines out of the reach of children. Stop use and ask a doctor if condition worsens or symptoms become worse after more than 7 days of treatment.

Reported adverse events (FAERS/openFDA)#

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