FDA label 82552cbf-3a73-877c-e053-2991aa0a7a66

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
dfe15c5d-40b8-4be8-82b8-c583b04803d5
SPL ID
82552cbf-3a73-877c-e053-2991aa0a7a66
Version
3
Effective date
2019-02-20
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:10:30

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 •in the eyes •over large areas of the body or on deep puncture wounds, animal bites or serious burns •in large quantities, particularly over raw surfaces or blistered areas. Stop use and ask a doctor if •the condition gets worse •the condition clears up and recurs within a few days •condition persists longer than 7 days •if pregnant or breast feeding, •ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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