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: 2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:23:30

Harmonized routes table
Harmonized routes
TOPICAL

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		POWERECT Lidocaine Male Delay	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		SKINS SEXUAL HEALTH LIMITED	openfda.manufacturer_name
ndc	package	81923-366-00	openfda.package_ndc
ndc	product	81923-366	openfda.product_ndc
ndc11	package	81923036600	derived:openfda.package_ndc
spl id		0976dfc5-c35a-11fe-e063-6294a90aa2bb	id
spl set id		42e0c40f-1efd-45ef-815d-53d193d720eb	set_id
unii		V13007Z41A	openfda.unii

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, 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.

Reported adverse events (FAERS/openFDA)#

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