FDA.reportPublic FDA data

FDA label cc83a07a-8d34-9fba-e053-2a95a90a0dae

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
74bbc671-2b5c-400b-8c91-f47933e0b679
SPL ID
cc83a07a-8d34-9fba-e053-2a95a90a0dae
Version
2
Effective date
2021-09-21
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 23:08:59

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 or mucus membranes. • Do not bandage tightly. • Do not apply to wounds or damaged skin. Stop use and ask a doctor if • Condition worsens. • Symptoms persist for more than 7 days or clear up and occur again within a few days. • Excessive irritation of skin develops. If pregnant or breastfeeding , ask a health professional before use.