FDA label a476ab54-a11f-4275-913b-b3eaf6f816ed

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
0e2aa14e-9c2a-45f5-8fb9-71abac7a655e
SPL ID
a476ab54-a11f-4275-913b-b3eaf6f816ed
Version
6
Effective date
2022-02-18
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:48:11

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 Use only as directed. For external use only. Do not use with other sprays, ointments, creams, or liniments. Do not apply to irritated skin and discontinue use if excessive skin irritation develops. Do not bandage. Do not use with heating pads or devices. When using this product avoid contact with the eyes or mucous membranes. Ask your physician before using on children under two years of age, or if you are pregnant, nursing, or have sensitive skin. If condition worsen, or if symptoms persist for more than 7 days, or clear up and then recur within a few days, stop use and contact your physician.

Reported adverse events (FAERS/openFDA)#

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