clean force
Generic: benzalkonium chloride
Labeler: ecolab inc.Drug Facts
Product Profile
Brand Name
clean force
Generic Name
benzalkonium chloride
Labeler
ecolab inc.
Dosage Form
LIQUID
Routes
Active Ingredients
benzalkonium chloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
47593-586
Product ID
47593-586_01db35ae-f9cd-44c0-8cd2-a4d60dd3c2cd
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2017-12-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
47593586
Hyphenated Format
47593-586
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
clean force (source: ndc)
Generic Name
benzalkonium chloride (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 750 mL in 1 BOTTLE, PLASTIC (47593-586-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "01db35ae-f9cd-44c0-8cd2-a4d60dd3c2cd", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1038799"], "spl_set_id": ["3f1ccba5-fc68-4e9b-8122-71b45dfa1282"], "manufacturer_name": ["Ecolab Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "750 mL in 1 BOTTLE, PLASTIC (47593-586-41)", "package_ndc": "47593-586-41", "marketing_start_date": "20171220"}], "brand_name": "Clean Force", "product_id": "47593-586_01db35ae-f9cd-44c0-8cd2-a4d60dd3c2cd", "dosage_form": "LIQUID", "product_ndc": "47593-586", "generic_name": "Benzalkonium chloride", "labeler_name": "Ecolab Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Clean Force", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20171220", "listing_expiration_date": "20261231"}