FDA label 173e02be-c458-45f1-9898-7639f902c191

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
16553eda-ec34-485a-a11c-f51260efd9fa
SPL ID
173e02be-c458-45f1-9898-7639f902c191
Version
1
Effective date
2026-09-03
Source export date
2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:48:37

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. Read all warnings and directions before use. Test first on small area of skin. Keep out of the reach of children. Do not Use : On wounds or damaged skin When using this product You may experience a burning sensation. The intensity of this reaction varies among individuals and may be severe. With regular use, this sensation generally disappears after several days. Avoid contact with the eyes, lips, nose and mucous membranes Do not tightly wrap or bandage the treated area Do not apply heat to the treated area immediately before or after use Stop use and ask a doctor if Condition worsens or does not improve after regular use

Reported adverse events (FAERS/openFDA)#

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