FDA.reportPublic FDA data

POWERECT Lidocaine Male Delay

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)

Brand name
POWERECT Lidocaine Male Delay
Generic name
LIDOCAINE HYDROCHLORIDE
Manufacturer
SKINS SEXUAL HEALTH LIMITED
Product type
HUMAN OTC DRUG
SPL set ID
42e0c40f-1efd-45ef-815d-53d193d720eb
SPL ID
0976dfc5-c35a-11fe-e063-6294a90aa2bb
Version
2
Effective date
2023-11-06
Source export date
2026-08-01
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/2026-08-01/d245bd7ce31d1d8ed63276109973402ece6c44860774da30f25b731cd7418983/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:32:09
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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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, when used as directed, does not provide relief, • If you or your partner develop a rash or irritation, such as burning or itching, discontinue use and consult a physician. discontinue use and consult a physician. FOR EXTERNAL USE ONLY. Avoid contact with eyes. Keep out of reach of children. • If product is swallowed, get medical attention or contact poison control center immediately. Do not use • on broken or inflamed skin, if partner is pregnant, on large areas of the body, or orally.