FDA label e9705790-82fd-4d43-9438-5a3e88ba9a67

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
ab757ae5-108d-418b-b37c-e46c3ff37fbc
SPL ID
e9705790-82fd-4d43-9438-5a3e88ba9a67
Version
6
Effective date
2018-01-17
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:22:28

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 Allergy Alert: Do not use if allergic to any of the ingredients. Do not use in eyes or on large areas of the body. Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns. When using this product, do not use longer than 1 week, unless directed by a doctor. Stop use and ask a doctor if condition lasts or gets worse, rahs or other allergic reaction develops.

Reported adverse events (FAERS/openFDA)#

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