Home NDC 71683-010-01 NDC 71683-010-01 - No Rush Desensitizing This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 71683-010
Requested NDC 71683-010-01
Package NDCs from labels 71683-010-02, 71683-010-01
Manufacturer CC Wellness LLC
Effective date 2026-10-06
Current FDA listing Not matched in FDA.report NDC product tables
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 72 of 188 · 3,742 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Walgreens Maximum Strength BENZOCAINE Walgreens 2ef0eb2c-b614-44e2-b9b3-97b02c654977 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 Toothache and Gum Relief Cushions BENZOCAINE Rite Aid 9970d485-0b78-1438-e053-2995a90ad32c 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 Nighttime 4X Medicated Cream BENZOCAINE Rite Aid 21645ed1-2dc0-223a-e063-6394a90ab021 2025-11-21 Warnings Exact identifier application number: M017 unii: U3RSY48JW5 4x Medicated Gum Cream BENZOCAINE Albertsons b81a308c-9c30-0e3d-e053-2a95a90a15d2 2025-11-21 Warnings Exact identifier application number: M017 unii: U3RSY48JW5 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC b0edd9d9-951f-d3dd-e053-2995a90a8d5a 2025-11-21 Warnings Exact identifier application number: M017 Eyewash Additive Concentrate WATER AND PROPYLENE GLYCOL Haws Corporation dd168403-398c-41ff-b1df-d93e4ff39de3 2025-11-20 Warnings Exact identifier unii: 6DC9Q167V3 unii: 059QF0KO0R Up up LIDOCAINE PAIN RELIEF MAXIMUM STRENGTH PATCHES Target Corporation 44121d40-86e1-0df6-e063-6294a90aedaf 2025-11-20 Warnings Exact identifier application number: M017 Up up PAIN RELIEF ADVANCED HYDROGEL PATCHES Target Corporation 44128b70-3172-ee37-e063-6294a90a705f 2025-11-20 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC f03090fa-f7e6-f53a-e053-2a95a90aa819 2025-11-20 Warnings Exact identifier application number: M017 HEATING PAIN RELIEF METHYL SALICYLATE, MENTHOL SUNSET NOVELTIES, INC ff073e47-3107-e17e-e053-6294a90a58fa 2025-11-20 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC fc8a8f20-97ab-481e-e053-6394a90a3525 2025-11-20 Warnings Exact identifier application number: M017 FOOT PAIN RELIEF ROLL-ON LIDOCAINE, MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 43edcea0-ab04-f368-e063-6294a90a817a 2025-11-19 Warnings Exact identifier application number: M017 Absolut Skin Corticosoothe Anti-Itch HYDROCORTISONE Absolut Skin Incorporated deb52218-9176-4aaa-a22f-b66dada6690f 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy LIDOCAINE InterMed Laboratories Private Limited 43f3d189-f6b7-02ed-e063-6394a90afd73 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch HealthA2Z LIDOCAINE InterMed Laboratories Private Limited 43f3e288-e828-8130-e063-6394a90a6d44 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch Leader LIDOCAINE InterMed Laboratories Private Limited 42f06914-c8b8-ea9c-e063-6294a90a79e6 2025-11-19 Warnings Exact identifier application number: M017 CVS Anti-Itch CAMPHOR, MENTHOL CVS 87715662-c788-9a8d-e053-2a95a90acb53 2025-11-19 Warnings Exact identifier application number: M017 Walgreen Anti Itch CAMPHOR, MENTHOL Walgreens b4f47a8d-d4a6-9233-e053-2a95a90afd90 2025-11-19 Warnings Exact identifier application number: M017 Leader Anti-Itch CAMPHOR, MENTHOL LEADER/Cardinal Helath 110, Inc. 9ca985c6-5017-0558-e053-2995a90a8202 2025-11-19 Warnings Exact identifier application number: M017 CVS Anti-Itch PRAMOXINE HCL CVS 87fc476a-5b12-7383-e053-2995a90a530b 2025-11-19 Warnings Exact identifier application number: M017
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.