FDA.reportPublic FDA data

FDA label 16ea284a-6805-4f0c-87b4-dde050e2c1f9

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
c70533ec-8a72-493a-bc2b-b5fe2281d0ec
SPL ID
16ea284a-6805-4f0c-87b4-dde050e2c1f9
Version
1
Effective date
2020-07-31
Source export date
2026-09-28
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/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:32:34

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

Warning For external use only. When using this product , Do not use into eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor , if irritation and redness develops; Condition persists for more than 72 hours Do not use In children less than 2 months of age; On open skin wounds. Other Information： use in well ventilated areas; keep away from heat/sparks//open flames/hot surfaces If swallowed, get medical help or contact a Poison Contrl Center right away.

Reported adverse events (FAERS/openFDA)#

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