FDA label e559c6c8-2976-77fb-e053-2995a90af43d

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
a1c9b818-eedc-8edb-e053-2a95a90a5a10
SPL ID
e559c6c8-2976-77fb-e053-2995a90af43d
Version
7
Effective date
2022-08-03
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 05:52:40

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 our ingredients. In your eyes, mouth, or eyes. If eye contact occurs, flush eyes with water. Ask a doctor before use if you have open wounds. serious burns. Stop use and ask doctor if redness or skin irritation develop after use, and persists for more than 72 hours. Keep out of reach of children Children should be supervised when using this product.

Reported adverse events (FAERS/openFDA)#

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