FDA label fefda55e-4ca9-4ae0-a9f1-3e36db41e251

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
91cf31f9-3e96-4cb8-991f-b1dbbfd6ef24
SPL ID
fefda55e-4ca9-4ae0-a9f1-3e36db41e251
Version
1
Effective date
2014-01-08
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:13:31

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 Stop use and ask a doctor if symptoms persist or worsen. If pregnant or breast-feeding , ask a healthcare professional before use. Keep out of reach of children . For external use only . Avoid using near eyes or mouth . In case if ingestion , seek medical attention immediately. Some individuals may be sensitive to essential oils. If irritation or reaction occurs, discontinue use.

Reported adverse events (FAERS/openFDA)#

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