FDA.reportPublic FDA data

FDA label 92e976d7-5f44-426c-8328-af0fc9c7fba5

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
7933360f-e548-438d-87d4-c9710e50befe
SPL ID
92e976d7-5f44-426c-8328-af0fc9c7fba5
Version
1
Effective date
2012-08-15
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:34:25

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 eyes •on wounds or damaged skin •on tightly bandaged skin Stop use and ask a doctor •if condition worsens •if symptoms last for more than 7 days •or clear up and return again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Directions Adults & Children Age 12: Apply to affected area not more than 3 to 4 times daily. Children under 12 years ask a doctor.

Reported adverse events (FAERS/openFDA)#

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