POWERECT Benzocaine Male Delay Gel

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 Benzocaine Male Delay Gel
Generic name: BENZOCAINE
Manufacturer: SKINS SEXUAL HEALTH LIMITED
Product type: HUMAN OTC DRUG
SPL set ID: 2fafe1f2-a31e-4b2a-bc51-81e16b319c3a
SPL ID: 1d5bbd54-69df-3338-e063-6294a90a53bf
Version: 3
Effective date: 2024-07-16
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:15:19

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		POWERECT Benzocaine Male Delay Gel	openfda.brand_name
generic name		BENZOCAINE	openfda.generic_name
manufacturer name		SKINS SEXUAL HEALTH LIMITED	openfda.manufacturer_name
ndc	package	81923-367-01	openfda.package_ndc
ndc	package	81923-367-00	openfda.package_ndc
ndc	product	81923-367	openfda.product_ndc
ndc11	package	81923036701	derived:openfda.package_ndc
ndc11	package	81923036700	derived:openfda.package_ndc
spl id		1d5bbd54-69df-3338-e063-6294a90a53bf	id
spl set id		2fafe1f2-a31e-4b2a-bc51-81e16b319c3a	set_id
unii		U3RSY48JW5	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, discontinue use and consult a physician. If you or your partner develop a rash or irritation, such as burning or itching, 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.

Reported adverse events (FAERS/openFDA)#

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