Home NDC 61010-5000-06 NDC 61010-5000-06 - 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 61010-5000-06
Package NDCs from labels 61010-5000-0, 61010-5000-1, 61010-5000-3, 61010-5000-4, 61010-5000-5, 61010-5000-6, 61010-5000-06
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 26 of 229 · 4,566 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pain Relief Gel-Patch LIDOCAINE AND MENTHOL Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. 0ae6cfd1-bbea-3fe6-e063-6294a90a541f 2026-05-17 Warnings Exact identifier unii: L7T10EIP3A Pain Relief Gel-Patch LIDOCAINE AND MENTHOL Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. 32e1df3a-2f8f-68df-e063-6294a90aa1d1 2026-05-17 Warnings Exact identifier unii: L7T10EIP3A Deep Blue Mini MENTHOL doTERRA International, LLC 51dd58a8-1fd5-9cd7-e063-6394a90a1f72 2026-05-15 Warnings Exact identifier application number: M017 CounterAct Cough Drops Orchard Cherry MENTHOL Melaleuca, Inc. 6049842c-d763-4a91-a225-976ed74e1693 2026-05-15 Warnings Exact identifier unii: L7T10EIP3A CounterAct Cough Drops Honey Lemon MENTHOL Melaleuca, Inc. 84ac3489-9d64-401f-ab78-715af4de5440 2026-05-15 Warnings Exact identifier unii: L7T10EIP3A Biofreeze Overnight Gel MENTHOL Reckitt Benckiser LLC f5c8c08b-c7c0-f84d-e053-2a95a90add15 2026-05-15 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Biofreeze Professional MENTHOL, UNSPECIFIED FORM Reckitt Benckiser LLC 00bba5d2-b0e0-701c-e063-6294a90a5741 2026-05-15 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Biofreeze Overnight Roll-on MENTHOL Reckitt Benckiser LLC f67d7b7a-8922-73f6-e053-2995a90a2e80 2026-05-15 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Biofreeze Overnight Relief MENTHOL, UNSPECIFIED FORM Reckitt Benckiser LLC 07be6e88-1850-4d6a-946d-f03830b8c4a2 2026-05-15 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Biofreeze Roll-On and Overnight Roll-On MENTHOL Reckitt Benckiser LLC 4d3dcb8f-2075-6bbc-e063-6394a90a4992 2026-05-15 Warnings Exact identifier application number: M017 Biofreeze Professional MENTHOL, UNSPECIFIED FORM Reckitt Benckiser LLC 6bef9ccb-7a5a-4c67-b1bc-a92b167312da 2026-05-15 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Biofreeze Roll-On MENTHOL Reckitt Benckiser LLC ebbbe9cb-b1ce-4dac-9fca-f54a2470c4fb 2026-05-15 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Biofreeze Precision Relief Pen MENTHOL Reckitt Benckiser LLC b4cc1db5-a33f-17bc-e053-2995a90ab7eb 2026-05-15 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Biofreeze Professional MENTHOL, UNSPECIFIED FORM Reckitt Benckiser LLC db982baf-31ea-4f09-90e3-cd5facb5dfe5 2026-05-15 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Biofreeze Professional Roll-On MENTHOL, UNSPECIFIED FORM Reckitt Benckiser LLC f62f8ec3-593d-480a-85a0-01fcd7f1790c 2026-05-15 Warnings Exact identifier application number: M017 unii: L7T10EIP3A PERFORM COOL AND SOOTHING PAIN RELIEVING ROLL-ON MENTHOL Reckitt Benckiser LLC 8af185ad-719e-4684-89c0-9c17c1277499 2026-05-15 Warnings Exact identifier application number: M017 unii: L7T10EIP3A PERFORM COOL and SOOTHING PAIN RELIEVING MENTHOL Reckitt Benckiser LLC ef158f63-2d75-47a3-b94a-2d821d511863 2026-05-15 Warnings Exact identifier application number: M017 unii: L7T10EIP3A KY Duration for Him LIDOCAINE Reckitt Benckiser LLC 83cc86bd-3303-4956-a198-fae85b6e34e1 2026-05-15 Warnings Exact identifier application number: M017 4% LIDOCAINE PATCHES 4% LIDOCAINE Shenzhen Huayuan Hengsheng Technology Co., Ltd. 4f53cfd3-a7c4-e308-e063-6294a90ad698 2026-05-14 Warnings Exact identifier application number: M017 Plantar Pain Relief Patch LIDOCAINE AND MENTHOL Guangzhou Sumi Technology Innovation Co., Ltd 4e8734db-e474-e1fa-e063-6394a90a3029 2026-05-14 Warnings Exact identifier unii: L7T10EIP3A
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.