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 112 of 228 · 4,549 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Nufabrx Calf Sleeve CAPSAICIN Nufabrx LLC bd9459c4-5596-746f-e053-2995a90a5400 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Arm Sleeve CAPSAICIN Nufabrx LLC a7993eaf-6488-a818-e053-2995a90a7ea6 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Back Wrap CAPSAICIN Nufabrx LLC e4f85ac8-57cb-46eb-e053-2995a90a9b1c 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Medicine Infused Socks CAPSAICIN Nufabrx LLC 013cb66f-8695-b69f-e063-6294a90a699c 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Neck Wrap CAPSAICIN Nufabrx LLC e10b420c-500d-5738-e053-2a95a90a008f 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Knee Sleeve CAPSAICIN Nufabrx LLC a5f455d4-5fc5-d516-e053-2a95a90a921e 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Medicine Infused Socks CAPSAICIN Nufabrx LLC 00d7d5bf-ee03-e73d-e063-6394a90a5d94 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Medicine Infused Elbow Sleeve CAPSAICIN Nufabrx LLC 27ef3ef0-2f98-6672-e063-6294a90aeca4 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Medicine Infused Wrist Sleeve CAPSAICIN Nufabrx LLC 22572cf9-fc0c-d327-e063-6394a90a2186 2025-10-15 Warnings Exact identifier application number: M017 Trilocaine LIDOCAINE HYDROCHLORIDE Trifluent Pharma LLC c58257bf-f06b-48d1-92df-a680dbd5eea0 2025-10-15 Warnings, Adverse reactions Exact identifier unii: V13007Z41A Antibacterial Lidocaine Wound Gel BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE WALGREENS eff77965-dc7f-49af-e053-2995a90a1a97 2025-10-14 Warnings Exact identifier application number: M017 unii: V13007Z41A Pleasure Balm Kama Sutra BENZOCAINE Cosmetic Enterprises Ltd f370e3c4-65ca-4f3c-a5aa-70e198e681a2 2025-10-14 Warnings Exact identifier application number: M017 Vanicream HC Anti-Itch HYDROCORTISONE Pharmaceutical Specialties, Inc. 28b06507-27a5-2cb1-e054-00144ff8d46c 2025-10-14 Warnings Exact identifier application number: M017 Sugar Free Cherry Fishermans Friend Menthol Cough Suppressant MENTHOL Lofthouse of Fleetwood, Ltd. 42d4bafb-b630-487e-b63d-13ad37a59454 2025-10-14 Warnings Exact identifier unii: L7T10EIP3A Trilogel LIDOCAINE HYDROCHLORIDE Trifluent Pharma LLC 22af7d63-6a56-4a38-a95b-0f88410b23cb 2025-10-14 Warnings Exact identifier application number: M017 unii: V13007Z41A PROINNATE Numbing Cream MENTHOL Guangzhou Haishi Biological Technology Co., Ltd. 40c63645-8ed3-82b3-e063-6294a90a5267 2025-10-13 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Cramergesic MENTHOL, METHYL SALICYLATE The Hygenic Company, LLC d0ffde7a-6942-74fc-e053-2a95a90a484a 2025-10-13 Warnings Exact identifier application number: M017 unii: L7T10EIP3A DENTI BUONGIORNO PLAQUE CARE TOOTH SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE ATOSAFE CO., Ltd 41155922-d7ac-0a7a-e063-6294a90afe48 2025-10-13 Warnings Exact identifier unii: 9E8X80D2L0 DENTI BUONGIORNO PLAQUE CARE TOOTH SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE DONG IL PHARMS CO.,LTD 41157552-2473-176b-e063-6294a90a9ad0 2025-10-13 Warnings Exact identifier unii: 9E8X80D2L0 DENTI BUONGIORNO GUM CARE TOOTH SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE ATOSAFE CO., Ltd 4115d122-3090-d3e5-e063-6294a90aafb6 2025-10-13 Warnings Exact identifier unii: 9E8X80D2L0
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.