FDA label 07414112-bec7-2e9a-e063-6294a90a3259

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: 7107e22e-9332-4509-b368-32296acb5648
SPL ID: 07414112-bec7-2e9a-e063-6294a90a3259
Version: 12
Effective date: 2023-10-08
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 05:31:43

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		07414112-bec7-2e9a-e063-6294a90a3259	id
spl set id		7107e22e-9332-4509-b368-32296acb5648	set_id

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. Use only as directed. Avoid contact with eyes and mucous membranes. If symptoms persist for more than 7 days, discontinue use and consult a physician If swallowed, consult a physician. Keep out of reach of children. Consult a physician prior to using on children under 12. Do not apply to open wounds or damaged skin. Do not use oils, lotions or powders on treatment area prior to application. Do not use with any bandage, wrap, stocking or similar device or garment. If pregnant or breast feeding, contact a physician prior to use.

Reported adverse events (FAERS/openFDA)#

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