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 93 of 114 · 2,277 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Univ of Vermont Medical Center Amenity BENZALKONIUM CHLORIDE AND SODIUM MONOFLUOROPHOSPHATE ASP Global, LLc 7841cfa9-e94e-4c3d-b5fb-676924017845 2024-12-17 Warnings Exact identifier application number: M003 Northside Hospital Mothers Vaginal ALCOHOL AND SODIUM MONOFLUOROPHOSPHATE ASP Global, LLc 7f1a85fd-086b-4fc7-abac-863dd3ea505a 2024-12-17 Warnings Exact identifier application number: M003 Mary Kay Satin Hands Shea Hand Sanitizer ALCOHOL Mary Kay Inc. b6c2b979-2940-1569-e053-2995a90a532c 2024-12-17 Warnings Exact identifier application number: M003 Foster and Thrive Decolorized Iodine ALCOHOL LIQUID Strategic Sourcing Services, LLC 2981529a-2bd0-3e9e-e063-6294a90a7236 2024-12-17 Warnings Exact identifier application number: M003 Foster and Thrive 2% Mild Iodine Tincture IODINE AND SODIUM IODIDE AND ALCOHOL LIQUID Strategic Sourcing Services, LLC 2981cb97-17de-ebda-e063-6394a90ad281 2024-12-17 Warnings Exact identifier application number: M003 Northside Hospital H.E.A.R.T. Strings Tote ALCOHOL AND SODIUM MONOFLUOROPHOSPATE ASP Global, LLc f8369a27-1995-4fdd-a282-35c344c11d83 2024-12-17 Warnings Exact identifier application number: M003 Northside Hospital Amenity Kit ALCOHOL AND SODIUM MONOFLUOROPHOSPATE ASP Global, LLc 877ce875-c5b0-4d9b-8f00-682914e3bc0e 2024-12-17 Warnings Exact identifier application number: M003 Wellstar Amenity BENZALKONIUM CHLORIDE AND SODIUM MONOFLUOROPHOSPHATE ASP Global, LLc ced9dd96-7922-43d7-906f-32afaad733ec 2024-12-17 Warnings Exact identifier application number: M003 Northside Hospital C-Section Mothers ALCOHOL AND SODIUM MONOFLUOROPHOSPHATE ASP Global, LLc 9df6d0e9-631c-4619-9d96-d2c5a32a590e 2024-12-17 Warnings Exact identifier application number: M003 Memorial Sloan Kettering Cancer Center Amenity Kit SODIUM MONOFLUOROPHOSPHATE ASP Global, LLc cab0bef1-f486-4eac-a61b-6030467d8650 2024-12-17 Warnings Exact identifier application number: M003 Sarasota Memorial Amenity ALCOHOL AND SODIUM MONOFLUOROPHOSPHATE ASP Global, LLc f5dda019-fcfd-4e99-89cc-e79e76b402e7 2024-12-17 Warnings Exact identifier application number: M003 Englewood Amenity BENZALKONIUM CHLORIDE AND SODIUM MONOFLUOROPHOSPHATE ASP Global, LLc 7c9ce1bf-6aa2-4073-ad09-2ddf845102a2 2024-12-17 Warnings Exact identifier application number: M003 Mentholatum Moisturizing Hand Sanitizer BENZALKONIUM CHLORIDE The Mentholatum Company 365c93bc-2299-4e69-ba3a-69414bfe78d7 2024-12-13 Warnings Exact identifier application number: M003 Curaplex Alcohol Prep Pad ISOPROPYL ALCOHOL Sarnova, Inc. da1a4baa-05eb-4a75-82bb-39c547daef64 2024-12-12 Warnings Exact identifier application number: M003 Foaming Hand Sanitizer ALCOHOL Empack Spraytech Inc. 8bb072f2-9cd4-499d-9d7f-7166451b8f20 2024-12-12 Warnings Exact identifier application number: M003 Extra Stength Hand Sanitizer Zytec Germ Buster ALCOHOL 80%W/W Empack Spraytech Inc. da854195-3a50-4fae-a5ea-183bf524c973 2024-12-12 Warnings Exact identifier application number: M003 Zytec Hand Sanitizer Wipes 80% w/w Alcohol ALCOHOL Empack Spraytech Inc. ab86fd0c-40cd-0bb6-e053-2a95a90a76e2 2024-12-12 Warnings Exact identifier application number: M003 Dermoplast Kids First Aid BENZETHONIUM CHLORIDE AND BENZOCAINE Advantice Health, LLC. 29a18018-5214-4080-ac40-e646319e95ce 2024-12-12 Warnings Exact identifier application number: M003 New Skin Bandage BENZETHONIUM CHLORIDE Advantice Health, LLC. 5846f414-8329-4034-b99f-92721bdb3d14 2024-12-12 Warnings Exact identifier application number: M003 CVS Hand Sanitizer ALCOHOL CVS b5faeb31-67c7-2000-e053-2995a90a1409 2024-12-10 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