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 138 of 151 · 3,010 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join PERSONAL CARE ICE COLD MENTHOL NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. 1994356c-e347-5b7d-e063-6394a90a476c 2024-01-01 Warnings Exact identifier application number: M017 Dendracin Neurodendraxcin METHYL SALICYLATE, MENTHOL AND CAPSAICIN Proficient Rx LP 7e765fc1-74c6-4af3-a9cf-05b57011d7d8 2024-01-01 Warnings Exact identifier application number: M017 CeraVe Developed with Dermatologists Itch Relief Moisturizing PRAMOXINE HYDROCHLORIDE L'Oreal USA Products Inc c6a0880e-fc16-46e9-8314-c56c9d15bf31 2023-12-31 Warnings Exact identifier application number: M017 CeraVe Developed with Dermatologists Anti Itch HYDROCORTISONE L'Oreal USA Products Inc. 8d65e945-2557-486f-9279-ecbaa08f31c4 2023-12-31 Warnings Exact identifier application number: M017 Nighttime Sleep-Aid Non-Habit Forming DIPHENHYDRAMINE HCI AptaPharma Inc. ed0ba7aa-e794-43da-b576-6b9945bf7477 2023-12-30 Warnings Exact identifier application number: M017 Sting-Kill BENZOCAINE AND MENTHOL RANDOB LABS, LTD. DBA CROSSINGWELL CONSUMER HEALTH b8bd9280-f20a-4b2a-aef7-a0ba7b3b8701 2023-12-29 Warnings Exact identifier application number: M017 Maybelline New York Baby Lips Dr Rescue Medicated Balm MENTHOL L'Oreal USA Products Inc 2f7b8221-66f6-4aed-8359-318cfc656a72 2023-12-28 Warnings Exact identifier application number: M017 Equate Cortisone HYDROCORTISONE 1% Walmart Inc 027fae33-93a0-a61f-e063-6294a90a990f 2023-12-27 Warnings Exact identifier application number: M017 Walgreens Cool n Heat Lidocaine LIDOCAINE HCL 4% Walgreens Co 0681c6c5-5a8b-ea9e-e063-6394a90a83bc 2023-12-27 Warnings Exact identifier application number: M017 EXTRA STRENGTH WAL-DRYL ITCH RELIEF DIPHENHYDRAMINE, ZINC ACETATE WALGREEN CO 681cf1af-2cc3-4e6d-b76f-f00731ea3e12 2023-12-27 Warnings Exact identifier application number: M017 XRay Pain Relief MENTHOL, (PLUS)-, CAMPHOR, (-)-, AND METHYL SALICYLATE Genomma Lab USA 5244ddee-fd9e-4df3-8fb3-b16aa321a316 2023-12-27 Warnings Exact identifier application number: M017 Camphor Spirit CAMPHOR 10% Pharma Nobis, LLC e42fbe63-b01c-4f85-e053-2a95a90a5143 2023-12-26 Warnings Exact identifier application number: M017 Equate Calaspray PRAMOXINE HCL 1%, ZINC ACETATE 0.1% Walmart Inc 027ed5ab-05ec-569f-e063-6394a90abbc3 2023-12-26 Warnings Exact identifier application number: M017 EXTERNAL ANALGESIC CAMPHOR, CAPSICUM, MENTHOL Hmong 21 3b6155a5-51aa-2780-e054-00144ff8d46c 2023-12-26 Warnings Exact identifier application number: M017 LEADER Camphor Spirit CAMPHOR (NATURAL) Cardinal Health, 110 dba Leader 7d3b0b28-5190-0622-e053-2991aa0af561 2023-12-22 Warnings Exact identifier application number: M017 Antiseptic Instant Pain Relief CAMPHOR 10.8% AND PHENOL 4.7% Pharma Nobis, LLC e42f484d-a642-3489-e053-2a95a90a4254 2023-12-22 Warnings Exact identifier application number: M017 Itch Relief Gel ITCH RELIEF GEL Pharma Nobis, LLC e42f484d-a641-3489-e053-2a95a90a4254 2023-12-22 Warnings Exact identifier application number: M017 Witch Hazel WITCH HAZEL Pharma Nobis, LLC e42f484d-a644-3489-e053-2a95a90a4254 2023-12-22 Warnings Exact identifier application number: M017 Dermoplast Pain relieving BENZOCAINE, MENTHOL Advantice Health dad00c95-4e11-3eec-e053-2a95a90a7a18 2023-12-21 Warnings Exact identifier application number: M017 equate Maximum Strength Pain Relieving 4% Lidocaine with Lavender Essential Oil Topical analgesic LIDOCAINE HYDROCHLORIDE Wal-Mart Stores, Inc. bf954949-a7b7-44ba-8565-f1d5c0a6c0d1 2023-12-21 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