endurance wipe

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: endurance wipe
Generic name: BENZOCAINE
Manufacturer: Absorption Pharmaceuticals, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 303db1de-94fc-4543-e063-6294a90a01b9
SPL ID: 56d1f6a0-5c3b-94f6-e063-6294a90a3ed5
Version: 8
Effective date: 2026-07-17
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 06:18:17

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		endurance wipe	openfda.brand_name
generic name		BENZOCAINE	openfda.generic_name
manufacturer name		Absorption Pharmaceuticals, LLC	openfda.manufacturer_name
ndc	package	55636-384-02	openfda.package_ndc
ndc	package	55636-384-03	openfda.package_ndc
ndc	package	55636-384-01	openfda.package_ndc
ndc	package	55636-384-04	openfda.package_ndc
ndc	product	55636-384	openfda.product_ndc
ndc11	package	55636038403	derived:openfda.package_ndc
ndc11	package	55636038402	derived:openfda.package_ndc
ndc11	package	55636038401	derived:openfda.package_ndc
ndc11	package	55636038404	derived:openfda.package_ndc
spl id		56d1f6a0-5c3b-94f6-e063-6294a90a3ed5	id
spl set id		303db1de-94fc-4543-e063-6294a90a01b9	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 · 3 matching rows.

warnings

Warnings For external use only. When using this product When using this product avoid contact with the eyes Stop use and seek 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. Symptoms persist.

warnings

When using this product When using this product avoid contact with the eyes

warnings

Stop use and seek 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. Symptoms persist.

Reported adverse events (FAERS/openFDA)#

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

endurance wipe

openFDA label record#

Harmonized identifier links#

Related Records#

Warnings cross-check#

warnings

warnings

warnings

Reported adverse events (FAERS/openFDA)#