Home NDC 81923-367 POWERECT Benzocaine Male Delay Gel
Product NDC 81923-367
11-digit product format 819230367
Labeler code 81923
Product ID 81923-367_1d5bbd54-69df-3338-e063-6294a90a53bf
Type HUMAN OTC DRUG
Nonproprietary name BENZOCAINE
Dosage form GEL
Route TOPICAL
Labeler SKINS SEXUAL HEALTH LIMITED
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-10-03
Substance BENZOCAINE
Active strength 50 mg/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base POWERECT Benzocaine Male Delay Gel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81923-367-00 POWERECT Benzocaine Male Delay Gel 3 mL in 1 PACKET GEL 3 3 81923-367-01 POWERECT Benzocaine Male Delay Gel 15 mL in 1 BOTTLE GEL 15 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81923-367 POWERECT BENZOCAINE MALE DELAY GEL (BENZOCAINE) GEL [SKINS SEXUAL HEALTH LIMITED] 3 Current NDC, Legacy NDC, 2 package rows 20240717_2fafe1f2-a31e-4b2a-bc51-81e16b319c3a.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 52 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Large Medicate Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE Amerisource Bergen a7d5f89b-59b9-4603-99aa-273b85be813e 2025-12-22 Warnings Exact identifier application number: M017 Good Neighbor Capsaicin Heat Patch for Back CAPSAICIN Amerisource Bergen f873a0b8-8123-1600-e053-6394a90a043e 2025-12-22 Warnings Exact identifier application number: M017 Good Neighbor Pharmacy Cold Therapy Pain Relief Patch MENTHOL Amerisource Bergen f872f371-b92c-f5d5-e053-6294a90a7dcd 2025-12-22 Warnings Exact identifier application number: M017 Caring Mills Hydrocortisone HYDROCORTISONE Veridian Healthcare b0b1889b-3099-4943-a4cb-d9a898a06860 2025-12-22 Warnings Exact identifier application number: M017 LIDOCAINE 5% LIDOCAINE Medhome Pharma Inc 46968f5a-d214-9871-e063-6394a90ab45d 2025-12-22 Warnings Exact identifier application number: M017 Blue-Emu THRIVE Cooling TRIPELENNAMINE 0.5% Kingsway Pharmaceuticals dba NFI, LLC 7ac6456a-42c5-4ac8-aae6-db4abfda9df0 2025-12-22 Warnings Exact identifier application number: M017 MENTHOL MENTHOL SUNSET PAIN RELIEF 45c5ca6f-d425-6cfb-e063-6394a90a1b66 2025-12-20 Warnings Exact identifier application number: M017 HERSTAT GST Genital Sore Treatment CAMPHOR, MENTHOL Herstat (USA) Inc. e8d27684-fb15-2e6a-e053-2a95a90a248f 2025-12-19 Warnings Exact identifier application number: M017 Kroger Anti Itch HYDROCORTISONE The Kroger Co 46547277-f11a-b9e7-e063-6294a90a2ccd 2025-12-19 Warnings Exact identifier application number: M017 Kroger Cool and Heat Roll-On MENTHOL Kroger 46551d07-3006-c3ec-e063-6294a90aa3f2 2025-12-19 Warnings Exact identifier application number: M017 Naughty Kitty Kat NO GAG DEEP THROAT SPRAY INKED SUGAR, INC 170eb644-c72c-5744-e063-6394a90a767d 2025-12-19 Warnings Exact identifier application number: M017 Tiger Balm Red Extra Strength CAMPHOR (SYNTHETIC) AND MENTHOL Haw Par Healthcare Ltd. ce703715-4c11-472c-9270-daac87b7be05 2025-12-19 Warnings Exact identifier application number: M017 Aspercreme with Lidocaine Foot Pain Creme LIDOCAINE HYDROCHLORIDE Chattem, Inc. da82cc0e-cc39-408e-87e1-c35bb6f9f51e 2025-12-19 Warnings Exact identifier application number: M017 Health Trak Plus Menthol-Infused Pain Relief Socks MENTHOL Railroad Sock LLC 43413e55-1db2-fc1a-e063-6394a90a7167 2025-12-18 Warnings Exact identifier application number: M017 BIO-ICE MENTHOL, CAMPHOR Electrostim Medical Services Inc. d/b/a EMSI 1bfd1468-9139-43b1-9709-d47b63d17cfb 2025-12-18 Warnings Exact identifier application number: M017 Lidotrode LIDOCAINE Strand Health Group 1fd20b9a-b8bc-c94f-e063-6394a90a2b69 2025-12-18 Warnings Exact identifier application number: M017 A Health Itch Relief Gel ITCH RELIEF GEL Bionpharma, Inc. ecf5decb-c98b-7739-e053-2995a90a5541 2025-12-18 Warnings Exact identifier application number: M017 After Burn 2.5% LIDOCAINE HCL Tender Corporation d/b/a Adventure Ready Brands 4640395f-a76c-d022-e063-6294a90adde6 2025-12-18 Warnings Exact identifier application number: M017 SPARTAN WIPES ENDURANCE WIPES TIV PRIME SRL 26d02431-2c95-001c-e063-6394a90a29c7 2025-12-18 Warnings Exact identifier application number: M017 Stopain Extra Strength Continuous MENTHOL Troy Manufacturing, Inc. a0f76968-d22c-4b1c-a9e6-8d0179a2e98e 2025-12-18 Warnings Exact identifier application number: M017
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 81923-367-00 81923036700 3 mL in 1 PACKET (81923-367-00) 3 ml 2022-10-03 0000-00-00 No No Current 81923-367-01 81923036701 15 mL in 1 BOTTLE (81923-367-01) 15 ml 2022-10-03 0000-00-00 No No Current