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 73 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 Mango Peach Splash ETHYL ALCOHOL MY IMPORTS USA LLC 3a2a4539-30eb-7451-e063-6294a90a2c22 2025-07-17 Warnings Exact identifier application number: M003 AshleyBelle Moisturizing Hand Sanitizer Sweet Floral Morning ETHYL ALCOHOL MY IMPORTS USA LLC 3a2a4fab-6776-7359-e063-6294a90a8524 2025-07-17 Warnings Exact identifier application number: M003 AshleyBelle Moisturizing Hand Sanitizer Coconut Sandalwood ETHYL ALCOHOL Zhejiang Guoyao Jingyue Aerosol Co., Ltd. 3a186822-025c-6970-e063-6394a90a5dc1 2025-07-16 Warnings Exact identifier application number: M003 X3 Clean Hand Sanitizer BENZALKONIUM CHLORIDE Natural Essentials, Inc. 5a0aea16-b1ff-4fa1-a292-0f1447474593 2025-07-15 Warnings Exact identifier application number: M003 Meridian Wrapped antibacterial deodorant BENZETHONIUM CHLORIDE Bob Barker Company Inc. 84aada12-f26e-4dc9-a256-8746c6431f61 2025-07-15 Warnings Exact identifier application number: M003 Meridian Unwrapped antibacterial deodorant BENZETHONIUM CHLORIDE Bob Barker Company Inc. 2c124769-a044-4d62-9325-89d5310a42de 2025-07-15 Warnings Exact identifier application number: M003 Isopropyl alcohol ISOPROPYL ALCOHOL AmerisourceBergen (Good Neighbor Pharmacy) 46122 5539cbe8-1d0f-41f8-9c5d-a9af7f28eed1 2025-07-15 Warnings Exact identifier application number: M003 HAND SANITIZER ALCOHOL ANTISEPTIC Kingkey MBC Life Technology Group Co.,Ltd 39a417a8-afec-f893-e063-6394a90a70ae 2025-07-11 Warnings Exact identifier application number: M003 HAND SANITIZER ALCOHOL ANTISEPTIC Kingkey MBC Life Technology Group Co.,Ltd 39a4aecf-1e74-4589-e063-6394a90a34fb 2025-07-11 Warnings Exact identifier application number: M003 HAND SANITIZER ALCOHOL ANTISEPTIC Kingkey MBC Life Technology Group Co.,Ltd 39a57c83-5ea6-5b36-e063-6294a90a284d 2025-07-11 Warnings Exact identifier application number: M003 terrasil First Aid Antiseptic Wound and Burn Care HEXYLRESORCINOL Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions 3cfa43a0-402b-4b32-94ff-2b2e2e6565c2 2025-07-11 Warnings Exact identifier application number: M003 Isopropyl Alcohol ISOPROPYL ALCOHOL Cardinal Health (Leader) 70000 bf355e30-ad2f-4f93-9d77-8efd6a908e58 2025-07-11 Warnings Exact identifier application number: M003 Isopropyl Rubbing Alcohol 70 Percent Wintergreen ISOPROPYL ALCOHOL Best Choice (Valu Merchandisers Company) abcc7941-e521-4ad6-89df-0b965b634eb3 2025-07-11 Warnings Exact identifier application number: M003 Isopropyl Alcohol ISOPROPYL ALCOHOL Cardinal Health (Leader) 70000 5ffa8ecf-1349-4758-8d47-e9a96d2ddaee 2025-07-11 Warnings Exact identifier application number: M003 XTRA Antibacterial Hand Fresh Lemon BENZALKONIUM CHLORIDE MY IMPORTS USA LLC. 39904847-ed55-f4a3-e063-6294a90a85a1 2025-07-10 Warnings Exact identifier application number: M003 XTRA Squeeze Antibacterial Hand Fresh Lemon BENZALKONIUM CHLORIDE Zhejiang Jifu Daily Chemical Co., Ltd. 397a897a-baab-d209-e063-6294a90aac65 2025-07-10 Warnings Exact identifier application number: M003 XTRA Antibacterial Hand Fresh Lemon BENZALKONIUM CHLORIDE Zhejiang Jifu Daily Chemical Co., Ltd. 398fd961-d5e6-9d40-e063-6294a90a5be5 2025-07-10 Warnings Exact identifier application number: M003 XTRA Squeeze Antibacterial Hand Fresh Lemon BENZALKONIUM CHLORIDE MY IMPORTS USA LLC. 39901012-e1a1-c6e3-e063-6294a90ab41f 2025-07-10 Warnings Exact identifier application number: M003 Aerowipe ALCOHOL WIPE Aero Healthcare 34c93704-9f3c-6746-e054-00144ff8d46c 2025-07-10 Warnings Exact identifier application number: M003 Walgreens 10 Povidone-Iodine Solution POVIDONE-IODINE WALGREEN COMPANY a7b635d0-9109-4cd6-9b96-fba0d76464fc 2025-07-10 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