FDA.reportPublic FDA data

Men Delay Wipe

Product NDC
82659-1000
11-digit product format
826591000
Labeler code
82659
Product ID
82659-1000_dd3ef1f5-4a3d-f09b-e053-2a95a90ade00
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine 3.5%
Dosage form
CLOTH
Route
TOPICAL
Labeler
Limitless Male Medical Clinic
Application
part348
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2022-04-20
Marketing end
0000-00-00
Substance
BENZOCAINE
Active strength
4 g/100g
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct82659-1000DDiscontinued by firm2026-10-05
excluded packagepackage82659-100082659-1000-1DDiscontinued by firm2026-10-05

Reported adverse events (FAERS/openFDA)#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82659-1000MEN DELAY WIPE (BENZOCAINE 3.5%) CLOTH [LIMITLESS MALE MEDICAL CLINIC]2Legacy NDC20231219_dd3ef094-37e5-46d5-e053-2995a90a45bb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82659-1000-1826591000018 PACKET in 1 BOX (82659-1000-1) > 1 g in 1 PACKET8 packet2022-04-200000-00-00NoNoCurrent