Home NDC 61010-5000-01 NDC 61010-5000-01 - Lidocaine Hydrochloride 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 61010-5000
Requested NDC 61010-5000-01
Package NDCs from labels 61010-5000-0, 61010-5000-1, 61010-5000-3, 61010-5000-4, 61010-5000-5, 61010-5000-6, 61010-5000-01
Manufacturer Safetec of America, Inc.
Effective date 2024-02-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type 61010-5000, Burn Gel Safetec of America, Inc. 2024-02-07 HUMAN OTC DRUG LABEL
FDA-Initiated Inactive NDC Indexing# NDC, Effective, Related label table NDC Effective Related label 61010-5000-0 2024-02-07 61010-5000, Burn Gel 61010-5000-1 2024-02-07 61010-5000, Burn Gel 61010-5000-3 2024-02-07 61010-5000, Burn Gel 61010-5000-4 2024-02-07 61010-5000, Burn Gel 61010-5000-5 2024-02-07 61010-5000, Burn Gel 61010-5000-6 2024-02-07 61010-5000, Burn Gel 61010-5000-0 2024-01-30 61010-5000, Burn Gel 61010-5000-1 2024-01-30 61010-5000, Burn Gel 61010-5000-3 2024-01-30 61010-5000, Burn Gel 61010-5000-4 2024-01-30 61010-5000, Burn Gel 61010-5000-5 2024-01-30 61010-5000, Burn Gel 61010-5000-6 2024-01-30 61010-5000, Burn Gel
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61010-5000-0 Lidocaine Hydrochloride 3.3 g in 1 PACKET GEL 3.3 5 61010-5000-1 Lidocaine Hydrochloride 121.2 g in 1 BOTTLE GEL 121.2 5 61010-5000-3 Lidocaine Hydrochloride 0.9 g in 1 POUCH GEL 0.9 5 61010-5000-4 Lidocaine Hydrochloride 144 in 1 CARTON GEL 144 5 61010-5000-4 Lidocaine Hydrochloride 0.9 g in 1 POUCH GEL 0.9 5 61010-5000-5 Lidocaine Hydrochloride 0.9 g in 1 POUCH GEL 0.9 5 61010-5000-5 Lidocaine Hydrochloride 25 in 1 CARTON GEL 25 5 61010-5000-6 Lidocaine Hydrochloride 0.9 g in 1 PACKET GEL 0.9 5 61010-5000-6 Lidocaine Hydrochloride 10 in 1 BOX GEL 10 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61010-5000 LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] 5 Current NDC, Legacy NDC, 9 package rows 20240208_1c5eb3b3-79b3-472a-ae36-ec6a7dc72925.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Lidocaine Hydrochloride ACTIVE INGREDIENT V13007Z41A LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] 2 Lidocaine ACTIVE MOIETY 98PI200987 LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] 2 .alpha.-tocopherol acetate INACTIVE INGREDIENT 9E8X80D2L0 LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] 2 aloe vera leaf INACTIVE INGREDIENT ZY81Z83H0X LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] 2 diazolidinyl urea INACTIVE INGREDIENT H5RIZ3MPW4 LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] 2 menthol INACTIVE INGREDIENT L7T10EIP3A LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] 2 propylene glycol INACTIVE INGREDIENT 6DC9Q167V3 LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] 2 trolamine INACTIVE INGREDIENT 9O3K93S3TK LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] 2 water INACTIVE INGREDIENT 059QF0KO0R LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] 2
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 229 · 4,566 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Target Lubricant Eye Drops High Performance POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL Target Corporation 6c449374-8847-4c4a-9073-1951ff31d404 2025-12-30 Warnings Exact identifier unii: 6DC9Q167V3 Kroger Pain Relief Lidocaine Patch LIDOCAINE Kroger Company f6407554-c9a7-24e2-e053-2a95a90aae02 2025-12-30 Warnings Exact identifier application number: M017 Kroger Hot and Cold Medicated Patch MENTHOL Kroger Company 0331c1dd-fe30-421a-85a7-6c6886e7ab27 2025-12-30 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Target Lubricant Eye Drops High Performance POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL Target Corporation ddc15dac-fbd8-42fa-80db-79f49fc6b9eb 2025-12-30 Warnings Exact identifier unii: 6DC9Q167V3 Menthol, Camphor MENTHOL, CAMPHOR Chemco Corporation 472fb097-92e5-c230-e063-6294a90ab33a 2025-12-30 Warnings Exact identifier application number: M017 unii: L7T10EIP3A MENTHOL MENTHOL CHEMCO CORPORATIOM 472fb99c-dcc2-d9a9-e063-6294a90a794c 2025-12-30 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Nufabrx Elbow Sleeve CAPSAICIN Nufabrx LLC 473004cd-f7f9-3c68-e063-6294a90a5b8a 2025-12-30 Warnings Exact identifier application number: M017 Nufabrx Leg Sleeve CAPSAICIN Nufabrx LLC 473015ed-3e0f-6eae-e063-6294a90a4c74 2025-12-30 Warnings Exact identifier application number: M017 Nufabrx Arm Sleeve CAPSAICIN Nufabrx LLC 472ef560-1ed6-c912-e063-6394a90aaa1c 2025-12-30 Warnings Exact identifier application number: M017 Nufabrx Shin Sleeve CAPSAICIN Nufabrx LLC 4730bf64-ea0c-ca8d-e063-6394a90af542 2025-12-30 Warnings Exact identifier application number: M017 Nufabrx Ankle Sleeve CAPSAICIN Nufabrx LLC 4730d164-9027-fff2-e063-6394a90a4280 2025-12-30 Warnings Exact identifier application number: M017 Nufabrx Knee Sleeve CAPSAICIN Nufabrx LLC 473098ca-02f1-c287-e063-6394a90a37e1 2025-12-30 Warnings Exact identifier application number: M017 PAIN RELIEF PATCHES LIDOCAINE Liberty Procurement, In 2d381c48-402f-4e46-81b2-41a184139a61 2025-12-30 Warnings Exact identifier application number: M017 Thera Care Pain Relief Menthol Patchs MENTHOL Veridian Healthcare 1faa1d4f-b7fb-4f36-aef1-2fedde114b8e 2025-12-30 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Lidocaine Pain Relief LIDOCAINE PAIN RELIEF Allegiant Health 7f715144-f0c8-48fc-a22d-eac85759c66a 2025-12-30 Warnings Exact identifier application number: M017 ONETOOTHCLINIC TOOTH SILICON DIOXIDE, TOCOPHEROL ACETATE, SODIUM PYROPHOSPHATE CONE MEDICAL Co., Ltd. 9a567c9e-b8ce-7bf1-e053-2995a90aff2b 2025-12-30 Warnings Exact identifier unii: 9E8X80D2L0 ONETOOTH CLINIC TOOTH SILICON DIOXIDE, TOCOPHEROL ACETATE, TETRASODIUM PYROPHOSPHATE CONE MEDICAL Co., Ltd. bd50abcd-8a85-2923-e053-2995a90a109b 2025-12-30 Warnings Exact identifier unii: 9E8X80D2L0 CVS Hydration Eye Drops POLYETYLENE GLYCOL 400, PROPYLENE GLYCOL CVS ecab8fa3-6575-0dde-e053-2a95a90abd61 2025-12-30 Warnings Exact identifier unii: 6DC9Q167V3 GoodSense Ultra Lubricant Eye Drops POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL Geiss, Destin & Dunn, Inc. 9b45ebb5-c43b-c9fb-e053-2a95a90a3411 2025-12-30 Warnings Exact identifier unii: 6DC9Q167V3 Medics Choice Fresh and Soothe Lubricant Eye Drops POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL KC Pharmaceuticals, Inc. 1f65b91a-4eac-65c2-e063-6394a90a0295 2025-12-30 Warnings Exact identifier unii: 6DC9Q167V3
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.