FDA.reportPublic FDA data

FDA label db5f7ecf-7590-45b0-e053-2a95a90ae9dd

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
619f858b-23fd-4bca-9077-5ecc04a1e350
SPL ID
db5f7ecf-7590-45b0-e053-2a95a90ae9dd
Version
5
Effective date
2022-03-29
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:25:25

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 Do not use: • in the eyes • internally • over large of the body • if you are allergic to any of the ingredients • longer than 1 week unless directed by a doctor Ask a doctor before use: • in case of deep or puncture wounds, animal bites, or serious burns Stop use and ask a doctor if: • the condition persists or gets worse • a rash or other allergic reaction develops Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately

Reported adverse events (FAERS/openFDA)#

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