Home NDC 71683-004-01 JO Prolonger with Benzocaine
Product NDC 71683-004
Requested package NDC 71683-004-01
11-digit product format 716830004
Labeler code 71683
Product ID 71683-004_3e9d73b4-5174-617d-e063-6294a90ad0e9
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form SPRAY
Route TOPICAL
Labeler CC Wellness LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-09-03
Substance BENZOCAINE
Active strength 7.5 g/100mL
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
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 JO Prolonger with Benzocaine
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 7.5 g/100mL
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71683-004-01 JO Prolonger with Benzocaine 1 in 1 BOX SPRAY 1 3 71683-004-02 JO Prolonger with Benzocaine 60 mL in 1 BOTTLE, SPRAY SPRAY 60 3
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 77 of 151 · 3,010 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ink Scribd Numbing LIDOCAINE HCL Prodigy Media Inc 54173858-aff0-43b2-bc7b-c4ecab9bc3e5 2025-09-17 Warnings Exact identifier application number: M017 Inkorporated Numbing LIDOCAINE HCL Prodigy Media Inc 3017056c-f3c6-4300-8344-bf6e7d32e870 2025-09-17 Warnings Exact identifier application number: M017 TattooGirl Numbing LIDOCAINE HCL Prodigy Media Inc 6abe4540-f6c9-412a-83f3-682df7715057 2025-09-17 Warnings Exact identifier application number: M017 Dr Tatty Numbing LIDOCAINE HCL Prodigy Media Inc 5bb558c1-bf8f-4956-8732-e19720f62f31 2025-09-17 Warnings Exact identifier application number: M017 Burn Ease Cooling LIDOCAINE ProStat First Aid LLC ec201ca1-efa0-4797-aec3-115647c29abd 2025-09-17 Warnings Exact identifier application number: M017 MedFreeze Naturally Cool Pain Relief MENTHOL MEDKO LLC 240f2346-c585-4334-997c-45db6268d7c4 2025-09-15 Warnings Exact identifier application number: M017 MEDISTIK DUAL HOT AND COLD METHYL SALICYLATE, MENTHOL Natureteq Inc. ba5f4626-f077-4a28-8dcc-dacd50741ead 2025-09-15 Warnings Exact identifier application number: M017 MEDISTIK ICE MENTHOL, CAMPHOR Natureteq Inc. c1077744-7b9a-4536-8faf-e21994a43ea5 2025-09-15 Warnings Exact identifier application number: M017 Caring Mills Vaginal Anti-Itch Cream BENZOCAINE, RESORCINOL Veridian Healthcare cd379e74-2841-47e4-b95a-de1b341b397f 2025-09-15 Warnings Exact identifier application number: M017 Lidocaine-Pain-Relief-Patch LIDOCAINE-PAIN-RELIEF-PATCH Henan Enokon Medical Instrument Co., Ltd. 3ecfa867-50f6-d98a-e063-6394a90aefa0 2025-09-14 Warnings Exact identifier application number: M017 Meijer Hydrocortsione Cream HYDROCORTSIONE CREAM 1% Meijer Distribution Inc. 1cbddb7e-f2e3-0951-e063-6394a90a3d37 2025-09-12 Warnings Exact identifier application number: M017 JO Prolonger with Benzocaine BENZOCAINE CC Wellness LLC d955f612-1267-f1be-e053-2995a90a5345 2025-09-12 Warnings Exact identifier application number: M017 ndc (package): 71683-004-01 ndc (product): 71683-004 ndc11 (package): 71683000401 JO for Him Prolonger with Lidocaine LIDOCAINE CC Wellness LLC b12dc6a3-142d-3219-e053-2995a90aead0 2025-09-12 Warnings Exact identifier application number: M017 Walgreens Medicated Foot Powder MENTHOL Davion, Inc 58e1e7f7-6284-411f-9765-0e63eabca0f3 2025-09-12 Warnings Exact identifier application number: M017 PAIN RELIEF PATCHES LIDOCAINE Amerisource Bergen 614f1e56-891f-4620-be10-0c075a1dbc3f 2025-09-11 Warnings Exact identifier application number: M017 Industrial Itch and Pain Relief DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE R & R Lotion, Inc 236415fc-f923-4a82-b54a-ecaf666dd2e0 2025-09-11 Warnings Exact identifier application number: M017 Eco Lips Menthol Medicated Lip Balm MENTHOL Eco Lips, Inc. fc4c25d6-6109-dfd8-e053-6394a90a4e91 2025-09-10 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE 1% Encube Ethicals, Inc. d6f5c0df-6262-4704-bb24-430f66bb2ca8 2025-09-09 Warnings Exact identifier application number: M017 Blue-Emu Lidocaine Pain Relief Cream LIDOCAINE CREAM 4% Kingsway Pharmaceuticals dba NFI, LLC 592811f2-e21c-6a58-e053-2991aa0a69a9 2025-09-09 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE Unifirst First Aid Corporation 282ed5ef-8c2a-4092-9d99-1a7eee7a39e3 2025-09-09 Warnings Exact identifier application number: M017
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 71683-004-01 71683000401 1 BOTTLE, SPRAY in 1 BOX (71683-004-01) / 60 mL in 1 BOTTLE, SPRAY (71683-004-02) 2015-09-03 0000-00-00 No No Current