FDA label 9aa072fa-2c91-d2ea-e053-2995a90a8455

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
5fe81556-5b5f-4765-9136-796e4974aed0
SPL ID
9aa072fa-2c91-d2ea-e053-2995a90a8455
Version
3
Effective date
2019-12-26
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 05:23:21

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. Do not use face or genital areas on a reas of blistered or broken skin with a compress after application When using this product do not get into eyes if contact occurs, flush eyes with water Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days. If pregnant or breastfeeding ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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