FDA label cc338a6c-01d3-7e30-e053-2995a90af168

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
3c08eccb-e923-44c6-b514-38f3eca81eb2
SPL ID
cc338a6c-01d3-7e30-e053-2995a90af168
Version
1
Effective date
2021-09-17
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:52:25

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.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.