skin cleanser
Generic: chloroxylenol
Labeler: west coast paper companyDrug Facts
Product Profile
Brand Name
skin cleanser
Generic Name
chloroxylenol
Labeler
west coast paper company
Dosage Form
SOAP
Routes
Active Ingredients
chloroxylenol 3.75 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72528-141
Product ID
72528-141_26e610c7-275e-c095-e063-6394a90a9d9d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2022-08-25
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72528141
Hyphenated Format
72528-141
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
skin cleanser (source: ndc)
Generic Name
chloroxylenol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3.75 mg/mL
Packaging
- 3785 mL in 1 BOTTLE, PUMP (72528-141-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "26e610c7-275e-c095-e063-6394a90a9d9d", "openfda": {"unii": ["0F32U78V2Q"], "rxcui": ["1362618"], "spl_set_id": ["e714abd6-8469-c43a-e053-2995a90a6956"], "manufacturer_name": ["West Coast Paper Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3785 mL in 1 BOTTLE, PUMP (72528-141-04)", "package_ndc": "72528-141-04", "marketing_start_date": "20220825"}], "brand_name": "Skin Cleanser", "product_id": "72528-141_26e610c7-275e-c095-e063-6394a90a9d9d", "dosage_form": "SOAP", "product_ndc": "72528-141", "generic_name": "Chloroxylenol", "labeler_name": "West Coast Paper Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Skin Cleanser", "active_ingredients": [{"name": "CHLOROXYLENOL", "strength": "3.75 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220825", "listing_expiration_date": "20261231"}