FDA label 0d8128c5-9bfb-c706-e063-6294a90a1aa0

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
0d81120b-f39e-bcde-e063-6294a90a70b7
SPL ID
0d8128c5-9bfb-c706-e063-6294a90a1aa0
Version
1
Effective date
2023-12-27
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:54:55

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 If you are allergic to any of the ingredients In eyes Over large areas of the body Ask a Doctor before Use Ask Doctor before use if you have: Deep or puncture wouns Animal bites Serious burns When using this product use only as directed Stop Use and ask a Doctor if: You need to use longer than 1 week Condition persists or gets worse rash or other allergic reaction develops Keep out of Reach of Children If Swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

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