FDA.reportPublic FDA data

FDA label 1fac82ef-e65b-4cc5-b04c-4e2cf1c823c7

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
8f812286-cb6e-42ae-b141-c3a3e55ad2fc
SPL ID
1fac82ef-e65b-4cc5-b04c-4e2cf1c823c7
Version
3
Effective date
2022-01-17
Source export date
2026-08-01
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/63703fa640102c69d41ceeb8d73f46d0a0be448587814b2aeca60b43bed7e054/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:37:35

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 bandage tightly Do not use On wounds or damaged skin or if you are allergic to ingredients in this product. Discontinue use and consult a physician if: Condition worsens or if symptoms persists for more than 7 days or clear up and occur again within a few days