FDA label 86f31e92-c25a-465d-bb5b-cf63894a6866

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
4cc45fa7-631f-4d0a-9310-cf2e0885d4a0
SPL ID
86f31e92-c25a-465d-bb5b-cf63894a6866
Version
2
Effective date
2012-09-05
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 06:11:31

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 if you are allergic to any ingredient in this product longer than one week unless directed by doctor. Stop use and ask doctor if condition persists or worsens symptoms persist for more than 7 days. Ask a doctor if used to treat deep or puncture wounds, animal bites or serious burns, you are pregnant or nursing. When using this product you may feel a brief stinging sensation when you apply it. The stinging should go away in short time. Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Reported adverse events (FAERS/openFDA)#

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