berberex wound cleanser

Generic: benzethonium chloride

Labeler: cosco international, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name berberex wound cleanser
Generic Name benzethonium chloride
Labeler cosco international, inc.
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

allantoin 5 g/1000mL, benzethonium chloride 1 g/1000mL

Manufacturer
Cosco International, Inc.

Identifiers & Regulatory

Product NDC 52261-0500
Product ID 52261-0500_d3e2c5a1-5f63-4c96-8fbe-1ba6c8c5d93d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M003
Listing Expiration 2026-12-31
Marketing Start 2015-05-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 522610500
Hyphenated Format 52261-0500

Supplemental Identifiers

RxCUI
1437628 1487627
UPC
0799475062131 0799475062148
UNII
344S277G0Z PH41D05744

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name berberex wound cleanser (source: ndc)
Generic Name benzethonium chloride (source: ndc)
Application Number M003 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 5 g/1000mL
  • 1 g/1000mL
source: ndc
Packaging
  • 118 mL in 1 BOTTLE, SPRAY (52261-0500-1)
  • 237 mL in 1 BOTTLE, SPRAY (52261-0500-2)
  • 473 mL in 1 BOTTLE, SPRAY (52261-0500-3)
source: ndc

Packages (3)

Ingredients (2)

allantoin (5 g/1000mL) benzethonium chloride (1 g/1000mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "d3e2c5a1-5f63-4c96-8fbe-1ba6c8c5d93d", "openfda": {"upc": ["0799475062131", "0799475062148"], "unii": ["344S277G0Z", "PH41D05744"], "rxcui": ["1437628", "1487627"], "spl_set_id": ["08b28f52-21fc-4694-a163-91c8193b4008"], "manufacturer_name": ["Cosco International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE, SPRAY (52261-0500-1)", "package_ndc": "52261-0500-1", "marketing_start_date": "20150824"}, {"sample": false, "description": "237 mL in 1 BOTTLE, SPRAY (52261-0500-2)", "package_ndc": "52261-0500-2", "marketing_start_date": "20150824"}, {"sample": false, "description": "473 mL in 1 BOTTLE, SPRAY (52261-0500-3)", "package_ndc": "52261-0500-3", "marketing_start_date": "20150824"}], "brand_name": "BerbereX Wound Cleanser", "product_id": "52261-0500_d3e2c5a1-5f63-4c96-8fbe-1ba6c8c5d93d", "dosage_form": "LIQUID", "product_ndc": "52261-0500", "generic_name": "Benzethonium Chloride", "labeler_name": "Cosco International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BerbereX Wound Cleanser", "active_ingredients": [{"name": "ALLANTOIN", "strength": "5 g/1000mL"}, {"name": "BENZETHONIUM CHLORIDE", "strength": "1 g/1000mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150517", "listing_expiration_date": "20261231"}