FDA label 60b9ff5f-7222-368e-e053-2a91aa0aaea1

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
fac11563-80ab-4339-ab2d-de53aa017154
SPL ID
60b9ff5f-7222-368e-e053-2a91aa0aaea1
Version
2
Effective date
2017-12-19
Source export date
2026-08-17
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/2026-08-17/f2a007a22a89560a66943d28521709913d039c2d0cd7e278faf1082cd194c72c/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
ca19d5b1416b6b66a9d383bfdc77d90e91adfeefe16ffcc1ac6b06ceb90d8d73
Import run
20260818T065550Z
Imported at
2026-08-18 07:13:23

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 do not use in or near the eyes. If contact occurs, rinse thoroughly with water. _________________________________ Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.