FDA.reportPublic FDA data

FDA label 064645f9-7b66-26bf-e063-6294a90af3ea

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
deb230e2-bfcc-ab51-e053-2995a90a3fea
SPL ID
064645f9-7b66-26bf-e063-6294a90af3ea
Version
2
Effective date
2023-09-26
Source export date
2026-08-01
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/0689a4374f1490600b5244071db3b04bd3bbc29ceda7a856edb8225323adf20a/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:01:10

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 THE EYES DO NOT APPLY TO WOUNDS OR DAMAGED SKIN DO NOT BANDAGE TIGHTLY DISCONTINUE USE OF THIS PRODUCY AND CONSULT A DOCTOR IF CONDITION WORSENS SYMPTOMS PERSIST FOR MORE THAN 7 DAYS SYMPTOMS CLEAR UP AND OCCUR AGAIN WITHIN A FEW DAYS IF PREGNANT OR BREAST FEEDING CONSULT A DOCTOR BEFORE USE DO NOT USE IF TAKING ANTICOAGULANTS OR HAVE BLEEDING DISORDERS.