FDA label 1aa4b4ee-90d2-0186-e063-6394a90a1a7e

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
68900b98-3d5e-633e-e053-2a91aa0a2a98
SPL ID
1aa4b4ee-90d2-0186-e063-6394a90a1a7e
Version
3
Effective date
2024-06-11
Source export date
2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:23:41

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. AVOID ANY FOODS CONTAMINATION DURING APPLICATION AND STORAGE. WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IN CASE OF CONTACT WITH EYES FLUSH THOROUGHLY WITH WATER. AVOID CONTACT WITH BROKEN SKIN. STOP USE AND ASK A DOCTOR IF IRRITATION OR REDNESS DEVELOPS OR CONDITION PERSISTS FOR MORE THAN 72 HOURS.

Reported adverse events (FAERS/openFDA)#

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