FDA label aaf7f1fa-e662-e629-e053-2995a90ae195

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
aaf7dc74-f114-6167-e053-2995a90aee79
SPL ID
aaf7f1fa-e662-e629-e053-2995a90ae195
Version
1
Effective date
2020-07-21
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:50:59

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 Do not apply this product to red and swollen skin, wound, or any part sensitive to it. Keep this product out of children’s reach. If swallowed, get medical help or contact a Poison Control Center immediately. For external use only. Avoid contact with eyes & wounded skin. Discontinue use if irritation and redness develop. If the condition persists for more than 72 hours, consult a physician. Store it in a cool and dry place. Flammable; avoid direct sunlight and open fire. And avoid contact with eyes and damaged skin.

Reported adverse events (FAERS/openFDA)#

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