Home NDC 76348-720 DermaRad Relief
Product NDC 76348-720
11-digit product format 763480720
Labeler code 76348
Product ID 76348-720_347e1804-127a-52a4-e063-6394a90ad676
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine Emulsion
Dosage form EMULSION
Route TOPICAL
Labeler RENU LABORATORIES, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-01-03
Substance ALLANTOIN; LIDOCAINE
Active strength 1.18; 4.72 g/118mL; g/118mL
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 · 16 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 76348-720-01 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 76348-720-01 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 76348-720-01 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 76348-720-01 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 76348-720-01 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 76348-720-01 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 76348-720-01 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product E Excluded after deficient or non-compliant submission was not corrected fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 76348-720-01 E Excluded after deficient or non-compliant submission was not corrected fb8cb913e6d1…eb8c232b6be0…
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 DermaRad Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALLANTOIN 1.18 g/118mL LIDOCAINE 4.72 g/118mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 344S277G0Z Internal UNII lookup 98PI200987 Internal UNII 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 76348-720-01 DermaRad Relief 1 in 1 BOX EMULSION 1 7 76348-720-04 DermaRad Relief 118 mL in 1 TUBE EMULSION 118 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76348-720 DERMARAD RELIEF (LIDOCAINE EMULSION) EMULSION [RENU LABORATORIES, LLC] 7 Current NDC, Legacy NDC, 2 package rows 20250508_d5e11f73-918b-eeac-e053-2995a90a4a83.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 51 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Certain Dri Clinical Strength Prescription Protection Rollon CERTAIN DRI CLINICAL STRENGTH PRESCRIPTION PROTECTION ROLLON Clarion Brands LLC 46a1f92e-4411-3989-e063-6394a90a7038 2025-12-23 Warnings Exact identifier application number: M017 PREMIERES PAIN MENTHOL Premiere Enterprises 128bd1e7-e961-416c-933b-fbd146e3d386 2025-12-23 Warnings Exact identifier application number: M017 PREMIERES PAIN MENTHOL Premiere Enterprises 35ff19df-4cc4-4fce-bd30-d87d835e0e26 2025-12-23 Warnings Exact identifier application number: M017 Premieres Pain MENTHOL Premiere Enterprises 1f081913-6106-4d06-a37a-631f710dbacb 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE jr. LIDOCAINE HCL, PHENOL Clarion Brands, LLC e1de73bb-917c-48d1-9a78-00c76edddb98 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE jr. PLUS Knee CAMPHOR, MENTHOL Clarion Brands, LLC 3ad8718d-ebf1-474f-8a91-48c78ab3b5c1 2025-12-23 Warnings Exact identifier application number: M017 Absorbine Jr. Plus MENTHOL Clarion Brands, LLC fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE JR PLUS ULTRA STRENGTH PAIN MENTHOL Clarion Brands, LLC cf329707-d90a-29dd-f2c2-acfd5af614f3 2025-12-23 Warnings Exact identifier application number: M017 Absorbine Jr Pro Cream LIDOCAINE HCL, PHENOL Clarion Brands, LLC 17b3f1e6-5554-4f3e-b133-76ae8ffea919 2025-12-23 Warnings Exact identifier application number: M017 Absorbine Jr Pro No Mess Roll-on Plus LIDOCAINE HCL, PHENOL Clarion Brands, LLC a7172f17-1525-4738-b72c-92479c730af2 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE JR MENTHOL Clarion Brands, LLC d656e7f6-ca26-1873-6c11-08aa82091bb0 2025-12-23 Warnings Exact identifier application number: M017 Relief Recovery METHYL SALICYLATE Mayway Corporation 27afd45e-2dc5-d099-e063-6394a90ad2b7 2025-12-23 Warnings Exact identifier application number: M017 Mobility METHYL SALICYLATE Mayway Corporation 27af9d17-9c15-5e2a-e063-6394a90aeda5 2025-12-23 Warnings Exact identifier application number: M017 medlot pain relief gel patch LIDOCAINE Lotfancy, Inc. 3ce4af20-b227-5b98-e063-6394a90ab992 2025-12-23 Warnings Exact identifier application number: M017 Nizoral Scalp Itch Relief HYDROCORTISONE Kramer Laboratories dba59238-6beb-447e-8c4c-e4bc00fd2c20 2025-12-23 Warnings Exact identifier application number: M017 Salonpas LIDOCAINE Pain Relieving LIDOCAINE Hisamitsu America, Inc. 63911880-8194-4c7d-a72f-cab94761b2d7 2025-12-23 Warnings Exact identifier application number: M017 The Body Builders Cream MENTHOL Smart Cookie Solutions f803325e-eb86-4b9e-a401-0a91bdcd6389 2025-12-22 Warnings Exact identifier application number: M017 PROINNATE Numbing Cream LIDOCAINE,MENTHOL Guangdong Aimu Biological Technology Co., Ltd 46895ddb-0b9f-675e-e063-6394a90adf23 2025-12-22 Warnings Exact identifier application number: M017 Caring Mills Vaginal Anti-Itch Cream BENZOCAINE, RESORCINOL Veridian Healthcare f2362658-aea2-438e-a66c-738022e6e047 2025-12-22 Warnings Exact identifier application number: M017 HealthWise Pain Relieving Menthol Gel MENTHOL 2% Veridian Healthcare 396d0fd4-67be-4de1-8f0c-42c83dfe9120 2025-12-22 Warnings Exact identifier application number: M017
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 76348-720-01 76348072001 1 TUBE in 1 BOX (76348-720-01) / 118 mL in 1 TUBE (76348-720-04) 1 tube 2022-01-03 0000-00-00 No No Current 76348-720-04 76348072004 118 mL in 1 TUBE 118 ml Historical