FDA label d58dd679-491f-3187-e053-2a95a90af875

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
e2755852-f27e-44bf-bcdd-64b69aea844d
SPL ID
d58dd679-491f-3187-e053-2a95a90af875
Version
2
Effective date
2022-01-14
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:16:07

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 the eyes Do not apply to wounds or damaged skin Do not bandage tightly Cap tube tightly and store at room temperature away from heat When using this product: do not use in large quantities particularly over raw surfaces or blistered areas do not exceed recommended doses unless recommended by a doctor Stop use and ask a doctor if: allergic reaction occurs condition worsens or does not improve within 7 days symptoms clear up and do not return within a few days you notice any unusual effects Keep out of the reach of children: If swallowed get medical help or call a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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