Home NDC 52261-0601 Berberex Wound Gel
Product NDC 52261-0601
11-digit product format 522610601
Labeler code 52261
Product ID 52261-0601_67cabb40-44f2-4ad0-ad14-77f4ab2bd1dc
Type HUMAN OTC DRUG
Nonproprietary name Benzethonium Chloride, Allantoin
Dosage form GEL
Route TOPICAL
Labeler Cosco International, Inc.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-07-01
Substance BENZETHONIUM CHLORIDE; ALLANTOIN
Active strength .0012; .005 kg/kg; kg/kg
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 · 14 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 52261-0601-1 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 52261-0601-1 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 52261-0601-1 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 52261-0601-1 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 52261-0601-1 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 52261-0601-1 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 52261-0601-1 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 Berberex Wound Gel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZETHONIUM CHLORIDE .0012 kg/kg ALLANTOIN .005 kg/kg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination PH41D05744 Internal UNII lookup 344S277G0Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 52261-0601-1 Berberex Wound Gel 0.0850 kg in 1 TUBE GEL 0.0850 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52261-0601 BERBEREX WOUND GEL (BENZETHONIUM CHLORIDE, ALLANTOIN) GEL [COSCO INTERNATIONAL, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20250331_5dd97e65-bfb3-468e-a2b1-e56d30da99df.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 1 of 117 · 2,333 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Burn Cream BENZALKONIUM CHLORIDE, LIDOCAINE HCI Trifecta Pharmaceuticals USA LLC e9a9fc7c-31da-ea3f-e053-2a95a90a0eab 2026-09-09 Warnings Exact identifier application number: M003 Alcohol Prep Pad Medium ALCOHOL PREP PAD Yangzhou Huanrui Medical Technology Co., Ltd 5af3eedc-d01e-c9e9-e063-6394a90a49e1 2026-09-08 Warnings Exact identifier application number: M003 Henry Schein Povidone-Iodine Prep Pad POVIDONE-IODINE Henry Schein, Inc. 313416b8-60b2-4a77-9b56-5c507aae9072 2026-09-08 Warnings Exact identifier application number: M003 Verifine ALCOHOL SWABS Promisemed Hangzhou Meditech Co., LTD 5af9f31b-0c92-e3a9-e063-6394a90a38c9 2026-09-08 Warnings Exact identifier application number: M003 Verifine ALCOHOL SWABS Promisemed Hangzhou Meditech Co., LTD 5afc0201-490e-ccf3-e063-6394a90aadad 2026-09-08 Warnings Exact identifier application number: M003 Sting Relief Pad BENZOCAINE, ISOPROPYL ALCOHOL CLOTH JINHUA JINGDI MEDICAL SUPPLIES CO., LTD 57ccc28b-5f5f-30ec-e063-6294a90a081c 2026-09-07 Warnings Exact identifier application number: M003 hand sanitizer - cherry sundae ALCOHOL Ganzhou Olivee Cosmetic Co., Ltd. 270d2ce0-6310-4a84-be8a-72db6062bae7 2026-09-07 Warnings Exact identifier application number: M003 hand sanitizer - vanilla frosting ALCOHOL Ganzhou Olivee Cosmetic Co., Ltd. f6cabda2-6e1c-4238-9a2e-df10e263517d 2026-09-07 Warnings Exact identifier application number: M003 hydrating mist hand sanitizer with silicone keychain holder - beaver nuggets ALCOHOL Ganzhou Olivee Cosmetic Co., Ltd. ba3612b3-9696-417a-ba66-eb9dc5ea27c6 2026-09-07 Warnings Exact identifier application number: M003 hydrating mist hand sanitizer with silicone keychain holder - signature scent ALCOHOL Ganzhou Olivee Cosmetic Co., Ltd. 5b0ac694-66e0-437f-86cd-09f259344b89 2026-09-07 Warnings Exact identifier application number: M003 Sweethearts - Crush On You - Peach Skin ALCOHOL Scent Theory Products LLC 5ac32582-d888-edf4-e063-6394a90a40ab 2026-09-05 Warnings Exact identifier application number: M003 Sweethearts - Be Mine - Sugared Berries ALCOHOL Scent Theory Products LLC 5ac32ffb-926a-f249-e063-6394a90a8d87 2026-09-05 Warnings Exact identifier application number: M003 Sweethearts - UR Sweet - Sweet Cherry Hand Sanitizer ALCOHOL Scent Theory Products LLC 5ac33b21-9192-8baa-e063-6294a90a6e75 2026-09-05 Warnings Exact identifier application number: M003 Sweethearts - Ooo La La - Banana Cream Hand Sanitizer ALCOHOL Scent Theory Products LLC 5ac34dda-fbdf-0ca7-e063-6394a90ab764 2026-09-05 Warnings Exact identifier application number: M003 SurviveX PREP WIPES ALCOHOL PREP PAD Changzhou Maokang Medical Products Co., Ltd. 5a7e9dc6-cf43-7ffc-e063-6394a90a3faa 2026-09-04 Warnings Exact identifier application number: M003 Members Mark ISOPROPYL ALCOHOL Sams West Inc c251ac50-f74f-4a48-e053-2a95a90aac0d 2026-09-04 Warnings Exact identifier application number: M003 Walmart ISOPROPYL ALCOHOL Walmart, Inc. 2f1342ef-1843-40a6-e063-6294a90a577f 2026-09-04 Warnings Exact identifier application number: M003 Curad Alcohol Prep Pads Medium ISOPROPYL ALCOHOL Medline Industries, LP 1ce3872e-2307-4a38-bd7d-7eb2b226cf3c 2026-09-04 Warnings Exact identifier application number: M003 Alcohol ISOPROPYL ALCOHOL SuperValu, Inc. 5e6e6d6f-4472-40f1-b0a9-96cee7ef075b 2026-09-04 Warnings Exact identifier application number: M003 Alcohol ISOPROPYL ALCOHOL Foodhold U.S.A. LLC a94c023c-5313-4940-90a7-b3061a8b90e1 2026-09-04 Warnings Exact identifier application number: M003
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 52261-0601-1 52261060101 .085 kg in 1 TUBE (52261-0601-1) 2022-07-01 0000-00-00 No No Current