FDA label 372a64a3-5fd7-470c-9810-fac1f9ada542

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
156eccfa-b515-4e69-9c72-2239dfcab5a1
SPL ID
372a64a3-5fd7-470c-9810-fac1f9ada542
Version
3
Effective date
2022-09-19
Source export date
2026-11-06
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/d46c999c1947092f6e18e5233482e6d1c02312c89d32ce906e3b19672a696546/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 08:05:21

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 and mucous membranes do not apply to wounds or damaged skin do not bandage tightly or use heating pad use only as directed Stop and ask a doctor if condition gets worse symptoms last more than 7 days symptoms clear up and occur again in a few days

Reported adverse events (FAERS/openFDA)#

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