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 19 of 115 · 2,286 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Smart Care Hand Sanitizer 4pk with Glitter Silicone Case - Watermelon Splash, Mango Papaya, Pineapple Sunrise, Coconut Water ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 529f25f9-92eb-b7df-e063-6294a90a8dbc 2026-05-25 Warnings Exact identifier application number: M003 Elf Hand Sanitizer Gift Set Maple Syrup Drizzle, Peppermint Sugar Rush, Creamy Vanilla Swirl ALCOHOL Scent Theory Products LLC 52aa188f-32b9-684a-e063-6294a90a8d4a 2026-05-25 Warnings Exact identifier application number: M003 Swab Applicator Brushes 8.3% w/w Povidone-Iodine and 72.5% w/w Isopropyl Alcohol (IPA) POVIDONE-IODINE, ISOPROPYL ALCOHOL XINXIANG XINDA TECHNOLOGY CO.,LTD 529b8ad6-081e-0ef8-e063-6294a90a67df 2026-05-24 Warnings Exact identifier application number: M003 Smart Care Hand Sanitizer with Glitter Silicone Case 2pk - Champagne Toast ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 529bc4a4-a7e3-dbcc-e063-6294a90a7bca 2026-05-24 Warnings Exact identifier application number: M003 Smart Care Hand Sanitizer with Glitter Silicone Case 2pk - Peach Bellini ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 529c5b79-bb85-0fb5-e063-6294a90ad8a0 2026-05-24 Warnings Exact identifier application number: M003 Smart Care Hand Sanitizer 4pk with Silicone Case Cherry Blossom,Gardenia,Lavender Vanilla,Coconut Honey ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 529cb9a6-3105-8a45-e063-6294a90ac5c1 2026-05-24 Warnings Exact identifier application number: M003 GLOBAL CARE GOLD ANTIBACTERIAL HAND BENZALKONIUM CHLORIDE GLOBAL IMPORT SALES LLC 30d4fa59-3b4c-a7fc-e063-6294a90aed05 2026-05-21 Warnings Exact identifier application number: M003 Hand Sanitizer ALCOHOL Guangdong Yanze Biotechnology Co., Ltd. 5251a3e8-f499-7775-e063-6294a90a44bf 2026-05-21 Warnings Exact identifier application number: M003 Hand Sanitizer ALCOHOL Guangdong Yanze Biotechnology Co., Ltd. 51ae09af-1ce4-2831-e063-6294a90ab6a5 2026-05-21 Warnings Exact identifier application number: M003 Walgreens 70% Isopropyl Alcohol Wipes ISOPROPYL ALCOHOL Walgreen Company e8b0ecc3-3a30-47c9-b7d1-518681d575b4 2026-05-21 Warnings Exact identifier application number: M003 Scentfull Midnight Air Hand Sanitizer ALCOHOL Scent Theory Products LLC 52561c01-574a-81e8-e063-6294a90a5f82 2026-05-21 Warnings Exact identifier application number: M003 THE WORLD OF Strawberry Shortcake ALCOHOL HAND SANITIZER Dongyang Loulee Cosmetics Co.,Ltd. 52581a49-181f-7db4-e063-6394a90a46f4 2026-05-21 Warnings Exact identifier application number: M003 First Aid Only Lidocaine Hydrochloride Analgesic Burn Gel LIDOCAINE HYDROCHLORIDE Acme United Corporation 5258cef2-0e5c-4ccd-e063-6394a90a9e5c 2026-05-21 Warnings Exact identifier application number: M003 FIGS evolvetogether Hand Sanitizer FIGS 01 Ginger - Cedar Scented ETHYL ALCOHOL Cosmetic Enterprises Ltd 525c16f9-e9e0-24ab-e063-6394a90a669d 2026-05-21 Warnings Exact identifier application number: M003 Smart Care Hand Sanitizer with Lip Gloss Strawberry ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 523a9ac5-3f80-ca8d-e063-6394a90ab5e7 2026-05-20 Warnings Exact identifier application number: M003 Smart Care Hand Sanitizer with Lip Gloss Watermelon ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 523b4aa4-e673-edb4-e063-6294a90a9054 2026-05-20 Warnings Exact identifier application number: M003 Smart Care Hand Sanitizer with Lip Gloss Care Bear ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 523b9b5a-30a0-1555-e063-6294a90abf91 2026-05-20 Warnings Exact identifier application number: M003 Smart Care Hand Sanitizer with Lip Gloss Polly Pocket ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 523bf360-16c7-e176-e063-6294a90a933f 2026-05-20 Warnings Exact identifier application number: M003 Hand Sanitizer ETHYL ALCOHOL Zhejiang Gaorong Cosmetic Co., Ltd. 523cd61a-c2ee-2c70-e063-6294a90a6c77 2026-05-20 Warnings Exact identifier application number: M003 70% Isopropyl Alcohol 70% ISOPROPYL ALCOHOL Greatdealson, Inc. 4aa809cd-500a-dd65-e063-6394a90a3144 2026-05-20 Warnings, Adverse reactions 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