FDA label 3cf6588d-0c0d-3ca5-e063-6294a90a64d6

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: 3cf69ae7-e067-8d57-e063-6394a90aec6a
SPL ID: 3cf6588d-0c0d-3ca5-e063-6294a90a64d6
Version: 1
Effective date: 2025-08-22
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:05:00

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		3cf6588d-0c0d-3ca5-e063-6294a90a64d6	id
spl set id		3cf69ae7-e067-8d57-e063-6394a90aec6a	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. Do not use if you or your partner are allergic to lidocaine or topical anesthetics. When using this product Avoid contact with the eyes Do not spray on broken, irritated, or sensitive skin. Stop and ask a doctor if This product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical supervision. You or your partner develop a rash or irritation, such as burning or itching. Ask a doctor or pharmacist before use If you have liver problems If your partner is, or may be pregnant.

Reported adverse events (FAERS/openFDA)#

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