Home NDC 52261-0500 BerbereX Wound Cleanser
Product NDC 52261-0500
11-digit product format 522610500
Labeler code 52261
Product ID 52261-0500_d3e2c5a1-5f63-4c96-8fbe-1ba6c8c5d93d
Type HUMAN OTC DRUG
Nonproprietary name Benzethonium Chloride
Dosage form LIQUID
Route TOPICAL
Labeler Cosco International, Inc.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-05-17
Substance ALLANTOIN; BENZETHONIUM CHLORIDE
Active strength 5; 1 g/1000mL; g/1000mL
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 · 28 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 52261-0500-2 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 52261-0500-3 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 52261-0500-1 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 52261-0500-2 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 52261-0500-3 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 52261-0500-1 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 52261-0500-2 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 52261-0500-3 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 52261-0500-1 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 52261-0500-2 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 52261-0500-3 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 52261-0500-1 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 52261-0500-3 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 52261-0500-1 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 52261-0500-2 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 52261-0500-3 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 52261-0500-1 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 52261-0500-2 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 52261-0500-3 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 52261-0500-1 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 52261-0500-2 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 Cleanser
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALLANTOIN 5 g/1000mL BENZETHONIUM CHLORIDE 1 g/1000mL
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 PH41D05744 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1437628 Internal RxNorm lookup 1487627 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 52261-0500-1 BerbereX Wound Cleanser 118 mL in 1 BOTTLE, SPRAY LIQUID 118 7 52261-0500-2 BerbereX Wound Cleanser 237 mL in 1 BOTTLE, SPRAY LIQUID 237 7 52261-0500-3 BerbereX Wound Cleanser 473 mL in 1 BOTTLE, SPRAY LIQUID 473 7
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ALLANTOIN ACTIVE INGREDIENT 344S277G0Z BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] 1 BENZETHONIUM CHLORIDE ACTIVE INGREDIENT PH41D05744 BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] 1 ALLANTOIN ACTIVE MOIETY 344S277G0Z BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] 1 BENZETHONIUM ACTIVE MOIETY 1VU15B70BP BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] 1 ALOE VERA WHOLE INACTIVE INGREDIENT KIZ4X2EHYX BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] 1 HYDRASTIS CANADENSIS WHOLE INACTIVE INGREDIENT R763EBH88T BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] 1 hydrogen peroxide INACTIVE INGREDIENT BBX060AN9V BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] 1 PANAX QUINQUEFOLIUS WHOLE INACTIVE INGREDIENT 0P067WOA1X BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] 1 water INACTIVE INGREDIENT 059QF0KO0R BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52261-0500 BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] 6 Current NDC, Legacy NDC, 3 package rows 20250331_08b28f52-21fc-4694-a163-91c8193b4008.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 77 of 114 · 2,277 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join AshleyBelle Moisturizing Hand Sanitizer Spearmint Eucalyptus ETHYL ALCOHOL 70% MY IMPORTS USA LLC 36b6d0e4-8d9f-9df5-e063-6294a90af326 2025-06-03 Warnings Exact identifier application number: M003 AshleyBelle Moisturizing Hand Sanitizer Sunflower Haze ETHYL ALCOHOL 70% MY IMPORTS USA LLC 36b71ebe-0638-73e8-e063-6394a90a9f4e 2025-06-03 Warnings Exact identifier application number: M003 AshleyBelle Moisturizing Hand Sanitizer Vanilla Cashmere ETHYL ALCOHOL 70% MY IMPORTS USA LLC 36b73e99-293a-865b-e063-6394a90a39c4 2025-06-03 Warnings Exact identifier application number: M003 Biopure 3 Hydrogen Peroxide HYDROGEN PEROXIDE Quest USA Corp 1e34d066-f82c-484c-87bf-aa54fb1fac07 2025-06-02 Warnings Exact identifier application number: M003 Simply Saline Wound Care BENZETHONIUM CHLORIDE 0.13% Church & Dwight Co., Inc. 6c802e91-b69e-cdd0-e053-2991aa0aa781 2025-06-01 Warnings Exact identifier application number: M003 HAND SANITIZER ALCOHOL ANTISEPTIC Kingkey MBC Life Technology Group Co.,Ltd 39a5a4a2-983e-a4e7-e063-6394a90aa27c 2025-06-01 Warnings Exact identifier application number: M003 BerbereX Wound Cleanser BENZETHONIUM CHLORIDE Cosco International, Inc. 08b28f52-21fc-4694-a163-91c8193b4008 2025-05-30 Warnings Exact identifier application number: M003 ndc (product): 52261-0500 Op-First Aid Series Povidone Iodine Prep Pad POVIDONE-IODINE Yiwu Ori-Power Medtech Co.,Ltd. 32dc994b-6636-72d8-e063-6294a90a98f6 2025-05-29 Warnings Exact identifier application number: M003 AshleyBelle Moisturizing Hand Sanitizer Apple Pear Clove ETHYL ALCOHOL 70% Zhejiang Guoyao Jingyue Aerosol Co., Ltd. 363e549a-c432-9f2e-e063-6394a90ae886 2025-05-28 Warnings Exact identifier application number: M003 Quality Choice Hydrogen Peroxide Wipes HYDROGEN PEROXIDE Chain Drug Marketing Association, Inc c2822eb6-8a2a-4337-acce-6f7fc8496175 2025-05-26 Warnings Exact identifier application number: M003 VLITEPRO First Aid Wipes ISOPROPYL ALCOHOL CLOTH Yiwu Ori-Power Medtech Co., Ltd. 35a7873a-e340-aae3-e063-6294a90a767f 2025-05-26 Warnings Exact identifier application number: M003 Band Aid Antiseptic Cleansing Liquid BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE Kenvue Brands LLC d2a6e0d2-5b9b-11c0-e053-2a95a90a4df0 2025-05-26 Warnings Exact identifier application number: M003 First Aid Only Antiseptic First Aid BENZALKONIUM CHLORIDE Acme United Corporation 35d06b38-55dd-e306-e063-6394a90aaf26 2025-05-23 Warnings Exact identifier application number: M003 BIOPURE20CT ANTI BACTERIAL HAND WIPES BENZALKONIUM CHLORIDE Zhejiang Furuisen Spunlaced Nonwovens Co., Ltd. 359f43c7-682a-ba1c-e063-6394a90a8dcb 2025-05-21 Warnings Exact identifier application number: M003 Walgreens Advanced Wound Wash BENZALKONIUM CHLORIDE Walgreens Co. 25c6d81c-d462-5a89-e063-6294a90a08f3 2025-05-20 Warnings Exact identifier application number: M003 Hand Sanitizer Cozy Comfort ALCOHOL Scent Theory Products LLC 35965496-d101-c604-e063-6294a90a1a48 2025-05-20 Warnings Exact identifier application number: M003 Hand Sanitizer Whipped Chai ALCOHOL Scent Theory Products LLC 35966f42-1f59-e5f5-e063-6294a90a9982 2025-05-20 Warnings Exact identifier application number: M003 VLITEPRO BZK Antiseptic Towelette BENZALKONIUM CHLORIDE Yiwu Ori-Power Medtech Co.,Ltd. 3543d2f6-16d3-aa65-e063-6294a90a9637 2025-05-19 Warnings Exact identifier application number: M003 Isopropyl Alcohol ISOPROPYL ALCOHOL Safeway, Inc. 29e5c152-15d7-4080-abf0-f76f8e9cbf5a 2025-05-16 Warnings Exact identifier application number: M003 Signature Care Advanced Hand Sanitizer ALCOHOL Yiwu Yangjie Daily Chemicals Co.,Ltd. db649f36-04b9-47f3-a334-94d3247f80de 2025-05-16 Warnings Exact identifier application number: M003
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 52261-0500-1 52261050001 118 mL in 1 BOTTLE, SPRAY (52261-0500-1) 118 ml 2015-08-24 0000-00-00 No No Current 52261-0500-2 52261050002 237 mL in 1 BOTTLE, SPRAY (52261-0500-2) 237 ml 2015-08-24 0000-00-00 No No Current 52261-0500-3 52261050003 473 mL in 1 BOTTLE, SPRAY (52261-0500-3) 473 ml 2015-08-24 0000-00-00 No No Current