FDA label 56da9d6a-984a-4d2b-8a1c-d23bfa573dcc

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
e6f217fc-d753-49f9-a467-b8bc7f7e7885
SPL ID
56da9d6a-984a-4d2b-8a1c-d23bfa573dcc
Version
11
Effective date
2018-10-12
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:22:46

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. When using this product: Avoid contact with eyes. DO NOT apply over deep or punctured wounds, infections or lacerations IF CONDITION WORSENS OR DOES NOT IMPROVE WITHIN 7 DAYS STOP USE AND CONSULT A PHYSICIAN. KEEP OUT OF REACH OF CHILDREN. In the event of accidental ingestion contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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