Home NDC 71105-500 Redicare Burn Gel
Product NDC 71105-500
11-digit product format 711050500
Labeler code 71105
Product ID 71105-500_2f9cfcad-603b-4de7-e063-6294a90a6172
Type HUMAN OTC DRUG
Nonproprietary name Redicare Burn Gel
Dosage form GEL
Route TOPICAL
Labeler Redicare LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-10-09
Substance LIDOCAINE HYDROCHLORIDE
Active strength 20 mg/g
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 26 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 71105-500-02 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 71105-500-02 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 71105-500-02 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 71105-500-02 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 71105-500-02 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 71105-500-02 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 71105-500-02 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 71105-500-02 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 71105-500-02 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 71105-500-02 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 71105-500-02 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 71105-500-02 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 71105-500-02 8dfbde2a14a4…c9ff85d89658…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Redicare Burn Gel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 20 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V13007Z41A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1011852 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71105-500-01 Redicare Burn Gel 3.3 g in 1 PACKET GEL 3.3 2 71105-500-02 Redicare Burn Gel 15 in 1 BOX GEL 15 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71105-500 REDICARE BURN GEL GEL [REDICARE LLC] 2 Current NDC, Legacy NDC, 2 package rows 20250308_947ac362-acfb-3508-e053-2a95a90a2873.zip
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 121 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ultra-Strength Pain Relief Analgesic CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM TARGET CORPORATION 159c5a84-bf68-41dd-a2d3-bc2402037244 2024-10-30 Warnings Exact identifier application number: M017 DG Health Cold n Hot Pain Relieving Topical Analgesic MENTHOL, UNSPECIFIED FORM Dolgencorp Inc 8fe13b85-ab74-42f8-a664-d3d2959921ac 2024-10-30 Warnings Exact identifier application number: M017 DEBACHERE Butt Balm After Care Antiseptic Pain Relief BENZOCAINE, BENZALKONIUM CHLORIDE DE.BACHERE USA LLC 8ba42864-69bf-455c-98d4-7f4ff94edceb 2024-10-29 Warnings Exact identifier application number: M017 Signature Care Hydrocortisone HYDROCORTISONE Safeway beefab66-b056-4bf1-b047-0780704ab87e 2024-10-29 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE H E B 15eb4676-5f6e-4c28-b5b9-4e45412dc37a 2024-10-29 Warnings Exact identifier application number: M017 Rael PAIN RELIEF ROLL-ON Analgesic CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM Rael, Inc. e6c49606-7c13-4dc6-a22d-ba54173ba788 2024-10-28 Warnings Exact identifier application number: M017 Monistat Care Instant Itch Relief BENZOCAINE Insight Pharmaceuticals LLC 4e9dc791-419f-4c79-aed4-760f8c17a5dd 2024-10-25 Warnings Exact identifier application number: M017 ZYLOTROL PAIN RELIEVING LIDOCAINE HCL, MENTHOL Asclemed USA, Inc. 1553351c-aee8-4c40-9548-35cce246bda9 2024-10-25 Warnings Exact identifier application number: M017 Outgro BENZOCAINE Medtech Products Inc. d6be8a1d-aca7-42b1-86da-881d42ffe8d5 2024-10-25 Warnings Exact identifier application number: M017 Monistat Complete Care Instant Itch Relief HYDROCORTISONE Insight Pharmaceuticals LLC a0f40504-6183-4f32-8d17-6586b3f386a6 2024-10-25 Warnings Exact identifier application number: M017 Boil Ease BENZOCAINE Insight Pharmaceuticals LLC bf108934-5e1a-4059-9dcf-008f52a83fab 2024-10-25 Warnings Exact identifier application number: M017 Dermarest Eczema Medicated HYDROCORTISONE Insight Pharmaceuticals LLC 0292ab62-5088-45fa-a056-70c2fcc19ef7 2024-10-25 Warnings Exact identifier application number: M017 anti itch HYDROCORTISONE Meijer, Inc. 2db7bcab-acb8-48ad-8cd1-842ff7765ed9 2024-10-23 Warnings Exact identifier application number: M017 NATUREANCE MIRACLE MENTHOL EROS GLOBAL CORP ec1a2a1f-a38d-9c59-e053-2a95a90ad268 2024-10-23 Warnings Exact identifier application number: M017 Profoot Plantar Relief Strips CAMPHOR (NATURAL), MENTHOL, METHYL SALICYLATE Rooftop Consumer Health, Inc. 65e142d8-da21-4c55-9faf-b387cb6c2c0e 2024-10-23 Warnings Exact identifier application number: M017 Profoot Pain Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE Rooftop Consumer Health, Inc. cc011b79-2761-40f7-8142-88f8e30a179a 2024-10-23 Warnings Exact identifier application number: M017 Profoot Pain Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE Profoot, Inc. 06f82bde-41a1-35f6-e063-6394a90a6437 2024-10-23 Warnings Exact identifier application number: M017 Deep Cover Bug Bite Relief BENZOCAINE Morrisons Outdoors, LLC 25010dd6-fb48-8ee7-e063-6394a90aee6c 2024-10-21 Warnings Exact identifier application number: M017 Evel Knievels Natural Choice Pain Relief MENTHOL, UNSPECIFIED FORM Natural Essentials, Inc. 4576656c-4b6e-6965-7665-6c52756c6573 2024-10-21 Warnings Exact identifier application number: M017 berkley and jensen anti itch HYDROCORTISONE BJWC 5cc6e4f6-c62d-4923-9726-9dbc569a3f49 2024-10-19 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 71105-500-01 71105050001 3.3 g in 1 PACKET 3.3 g Historical 71105-500-02 71105050002 15 PACKET in 1 BOX (71105-500-02) / 3.3 g in 1 PACKET (71105-500-01) 15 packet 2019-10-09 No No Current