FDA.reportPublic FDA data

FDA label 2812572d-00a8-0d61-e054-00144ff8d46c

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
51bafded-328c-4eba-b1a3-c9e50fa552f6
SPL ID
2812572d-00a8-0d61-e054-00144ff8d46c
Version
3
Effective date
2015-12-29
Source export date
2026-08-01
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/5a565ce64c898c83223b815b9579cd46fb0c6d54977c3cace2133e40124f7fbb/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:08:52

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 : Use only as directed Do not apply to open wonds or damaged skin Do not use with other ointments, creams, sprays or liniments After applying wash hands thoroughly with cool water Stop use and ask a doctor if: Condition worsens or symptoms persists for more than 7 days or clear up and recur Redness is present or irritation develops