FDA label aa5c207f-2da5-3a2e-e053-2a95a90abcf8

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
173d3114-6c8a-4089-9e0b-92a8d0fa5b3b
SPL ID
aa5c207f-2da5-3a2e-e053-2a95a90abcf8
Version
5
Effective date
2020-07-13
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:42:16

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

For external use only. Do not use near the eyes, mouth, ears or other sensitive areas of the body if contact occurs, rinse thoroughly with water apply over large areas of the body longer than 1 week unless directed by a doctor. Ask your doctor before use if you have deep or puncture wounds, animal bites, or serious burns. Stop use and ask a doctor if condition worsens or does not improve within 7 days. Keep out of reach of children. If wallowed, get mecial help or contact a Poison Control Center right away. It is recommended you skin patch test prior to use.

Reported adverse events (FAERS/openFDA)#

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