FDA label 629b06c5-67d9-3cea-e053-2991aa0a37db

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
b0bd2926-7766-45fc-9a95-3ff8c0a4fffc
SPL ID
629b06c5-67d9-3cea-e053-2991aa0a37db
Version
3
Effective date
2018-01-12
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:12:58

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: premature Ejaculation may be due to a condition requiring medical supervision. if this product, used as directed, does not provide relief, discontinue use and consult a doctor. For topical use only. Do not use if you or your partner are allergic to Lidocaine or topical anesthetics. Keep away from fire and flame. Discontinue use if you or your partner develop a rash or irritation, such as burning or itching. If symptoms persist, consult a doctor. Do not spray on broken, ittitated or sensitive skin. Avoid contact with eyes. For external use only. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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