FDA label d2a9b04b-c9e8-5cde-e053-2995a90a4e07

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
f435c3ed-f99b-4baf-af07-69780cd3ef9b
SPL ID
d2a9b04b-c9e8-5cde-e053-2995a90a4e07
Version
2
Effective date
2021-12-08
Source export date
2026-08-01
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/928e480b2a9ec5fd356ebc3e5dcca70f0f57b8a051cfbb174a4421de39bb77a2/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:26:29

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. Avoid contact with eyes. Do not use in large quantities, particularly over the raw surfaces or blistered area Stop use and ask a doctor if condition worsens, or if symptoms persists for more than 7 days or clear up and occur again within the few days. Discontinue use.