FDA label e919fb03-95e3-4f84-a642-b1cba8cc16dd

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
f7d0240c-b247-46a1-a0df-1ae429fa627c
SPL ID
e919fb03-95e3-4f84-a642-b1cba8cc16dd
Version
2
Effective date
2018-11-02
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:05:13

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 As with any drug, if you are pregnant or breast-feeding, ask a health professional before use. For external use only. Some individuals may be sensitive to essential oils, skin test for tolerability. If accidental ingestion more than several drops, and adverse reaction occurs, get medical help or contact a Poison Control Center. Do not apply to the eyes; in the event of contact, flush with water and seek advice from medical personnel. Keep all medicines out of the reach of children. Stop use and ask a doctor if condition worsens, symptoms last more than 7 days, or clear up and occur again within a few days.

Reported adverse events (FAERS/openFDA)#

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