FDA.reportPublic FDA data

FDA label 9842b6ca-34f3-e6f1-e053-2995a90a0bac

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
ba97c4ee-e097-4e9d-937a-f5ee4f9d6dfb
SPL ID
9842b6ca-34f3-e6f1-e053-2995a90a0bac
Version
3
Effective date
2019-11-26
Source export date
2026-08-01
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/8ac060fefb6f4d67c41cc2c9e4330286ca93c48094c18386c11bf706a1d8bd34/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:31:20

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 -in large quantities, particularly over raw surfaces or blistered areas When using this product -avoid contact with eyes Stop Use and ask a doctor -if condition worsens, or if symptoms persist for more than 7 days or clear up and then occur again within a few days, discontinue use of this product and consult a physician