Home NDC 71683-005 LubeLife Climax Control Delay
Product NDC 71683-005
11-digit product format 716830005
Labeler code 71683
Product ID 71683-005_3e62265a-9563-8fee-e063-6394a90a13d4
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 2022-01-01
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# Observed captured status history: Rows come only from successfully parsed FDA auxiliary ZIP captures. They show the state present in that artifact, not a continuous regulatory timeline. Absence before, after, or between captures is not proof of status, and a known non-data HTTP 403 capture is preserved in backfill provenance but cannot produce a status row.
Historic NDC status page 1 of 1 · 12 matching rows.
Browse every current auxiliary row. · Browse the complete NDC auxiliary source catalog.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-11-09 02:27 UTC · source 2024-11-08 excluded product product 71683-005 I Inactivated by FDA excluded / ndc_excluded.zip ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 71683-005 71683-005-01 I Inactivated by FDA excluded / ndc_excluded.zip ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 71683-005 I Inactivated by FDA excluded / ndc_excluded.zip 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 71683-005 71683-005-01 I Inactivated by FDA excluded / ndc_excluded.zip 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 71683-005 I Inactivated by FDA excluded / ndc_excluded.zip 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 71683-005 71683-005-01 I Inactivated by FDA excluded / ndc_excluded.zip 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 71683-005 I Inactivated by FDA excluded / ndc_excluded.zip 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 71683-005 71683-005-01 I Inactivated by FDA excluded / ndc_excluded.zip 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 71683-005 I Inactivated by FDA excluded / ndc_excluded.zip 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 71683-005 71683-005-01 I Inactivated by FDA excluded / ndc_excluded.zip 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 71683-005 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 71683-005 71683-005-01 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 153 · 3,056 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Icy Hot Original Nighttime Recovery Pain Relief No Mess Roll On MENTHOL Chattem, Inc. aa40c907-eeb5-4fda-b35e-439cbecc178c 2026-07-31 Warnings Exact identifier application number: M017 Aspercreme with Lidocaine Dry LIDOCAINE Chattem, Inc. 008abaaa-5e12-4246-a7f5-66f3966acf28 2026-07-30 Warnings Exact identifier application number: M017 Icy Hot Performance No-Mess Pain Relief Cream MENTHOL 16%, CAMPHOR 11% Chattem, Inc. 5e3e272a-c001-4f57-9535-521ccc85ae65 2026-07-30 Warnings Exact identifier application number: M017 Auixudin Lidocaine Pain Relief Gel-Patch LIDOCAINE PAIN RELIEF GEL-PATCH Henan Enokon Medical Instrument Co., Ltd. 57bc7b9e-e2f7-724b-e063-6394a90ab36f 2026-07-29 Warnings Exact identifier application number: M017 Jinfahe Lidocaine Pain Relief Patch LIDOCAINE PAIN RELIEF PATCH Henan Enokon Medical Instrument Co., Ltd. 57bcd9c5-767e-b634-e063-6394a90a2878 2026-07-29 Warnings Exact identifier application number: M017 Maximun Strength Lidocaine Patch Plus Menthol LIDOCAINE, MENTHOL Meijer Distribution Inc d0468514-58ea-4d8f-b634-a65bf95c0316 2026-07-29 Warnings Exact identifier application number: M017 Oudetas Lidocaine Cream LIDOCAINE CREAM Guangzhou Jingliang Cosmetics Co., Ltd. 57ca9220-2778-790a-e063-6294a90af506 2026-07-29 Warnings Exact identifier application number: M017 Aspercreme Lidocaine No-Mess plus Lavender LIDOCAINE HCL Chattem, Inc. 3948a3d2-ce04-4703-8709-211e75c9c38d 2026-07-29 Warnings Exact identifier application number: M017 LidoPro LIDOCAINE AND MENTHOL Clinic Pharma cdfd6b39-b430-4e95-a0f7-682cf3d78b52 2026-07-28 Warnings Exact identifier application number: M017 LidoPro Patch (Lidocaine 4%, Menthol 1%) LIDOCAINE AND MENTHOL PATCH Clinic Pharma 2b4d2105-b7ad-2695-e063-6394a90a999b 2026-07-28 Warnings Exact identifier application number: M017 Earths Care Pain Relieving CAMPHOR, MENTHOL, METHYL SALICYLATE DLC Laboratories, Inc. 5c3976da-a6cb-4b94-ae41-3e86b1ab13cb 2026-07-28 Warnings Exact identifier application number: M017 Muscle Rub Cream MENTHOL 10%, METHYL SALICYLATE 15% Preferred Pharmaceuticals Inc. 9e7568b6-52ae-4f7a-9bfd-503fd80a297e 2026-07-28 Warnings Exact identifier application number: M017 Aspercreme Lidocaine with Rosemary and Mint LIDOCAINE HYDROCHLORIDE Chattem, Inc. 9d40bfea-85d0-4943-83e9-0c16e79a011c 2026-07-28 Warnings Exact identifier application number: M017 KENS PAIN AND ARTHRITIS FORMULA MENTHOL Eezaway Relief Inc 35834473-3ad5-41ec-a110-e742aa7e2ee4 2026-07-28 Warnings Exact identifier application number: M017 DERMFREE Lidocaine 4% NUMBING Topical Anorectal Cream LIDOCAINE 4% NUMBING TOPICAL ANORECTAL CREAM Wenzhou Yuyuan Pharmaceutical Co., Ltd. 57935b64-6e2e-85d0-e063-6394a90a7428 2026-07-27 Warnings Exact identifier application number: M017 1% Hydrocortisone Anti-itch 1% HYDROCORTISONE ANTI-ITCH ALAINA HEALTHCARE PRIVATE LIMITED b8416467-55f7-4e5f-a5cb-3abd3e2bb577 2026-07-27 Warnings Exact identifier application number: M017 OWELL NATURALS ARTHRITIS MAXIMUM STRENGTH MENTHOL OWELL NATURAL 8 LLC 57984bc2-bf1d-c423-e063-6394a90a06ae 2026-07-27 Warnings Exact identifier application number: M017 Original Pain Relief TOPICAL ANALGESIC LOTION Real Time Pain Relief Inc 579bd303-9a50-4d66-e063-6294a90a6141 2026-07-27 Warnings Exact identifier application number: M017 Lidfix Pain Relief Patch Lidocaine LIDOCAINE HETERO HEALTHCARE LIMITED 2149f0e3-1983-4f02-929e-ecd20357f4bb 2026-07-27 Warnings Exact identifier application number: M017 RectoProtect LIDOCAINE Akron Pharma Inc. 1ca7d6cf-85a1-41a6-a07f-cff06a7edfbb 2026-07-27 Warnings Exact identifier application number: M017
Additional Listing Data#
Finished product Yes
Brand name base LubeLife Climax Control Delay
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 71683-005-01 LubeLife Climax Control Delay 1 in 1 BOX SPRAY 1 3 71683-005-02 LubeLife Climax Control Delay 60 mL in 1 BOTTLE, PLASTIC SPRAY 60 3
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71683-005-01 71683000501 1 BOTTLE, PLASTIC in 1 BOX (71683-005-01) / 60 mL in 1 BOTTLE, PLASTIC (71683-005-02) 2022-01-01 0000-00-00 No No Current 71683-005-02 71683000502 60 mL in 1 BOTTLE, PLASTIC 60 ml Historical