FDA label 2a31ef46-9581-45cd-ada8-33918ecfb6c1

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
5df9f7fa-2aa5-49c5-96af-d7f7c2ee476a
SPL ID
2a31ef46-9581-45cd-ada8-33918ecfb6c1
Version
2
Effective date
2021-11-08
Source export date
2026-11-06
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/2026-11-06/3b52cde3709f43d454872fcaffdb78395b270bc65272c06ef1005cc77c998864/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 09:04:42

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: For external use only When using this product: • Use only as directed. Read and follow all directions and warning on this carton • Do not bandage tightly • Avoid contact with eyes and mucous membranes • Do not use at the same time as other topical analgesics • Do not apply to wounds or sensitive skin • Do not remove when wet. Allow to dry and slowly remove Stop use and ask doctor if: • Condition worsens or if symptoms persist more than 7 days • Discontinue use of this product and consult a physician if you have sensitive skin or cancer • Consult a health professional before use if pregnant or breast feeding • Keep out of reach of children. If swallowed, get medical help or contact poison control right away

Reported adverse events (FAERS/openFDA)#

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