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
SOLUTION
Routes
Active Ingredients
benzalkonium chloride 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
47593-584
Product ID
47593-584_95962829-ae2f-4b3e-8f88-c9f78fbe33bc
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2017-06-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
47593584
Hyphenated Format
47593-584
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
- 5 mg/mL
Packaging
- 750 mL in 1 BOTTLE, PLASTIC (47593-584-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "95962829-ae2f-4b3e-8f88-c9f78fbe33bc", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1731737"], "spl_set_id": ["dc7bad8c-2e29-4d5d-b87e-8d9eae7c2c1c"], "manufacturer_name": ["Ecolab Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "750 mL in 1 BOTTLE, PLASTIC (47593-584-41)", "package_ndc": "47593-584-41", "marketing_start_date": "20170630"}], "brand_name": "Clean Force", "product_id": "47593-584_95962829-ae2f-4b3e-8f88-c9f78fbe33bc", "dosage_form": "SOLUTION", "product_ndc": "47593-584", "generic_name": "Benzalkonium Chloride", "labeler_name": "Ecolab Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Clean Force", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "5 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170630", "listing_expiration_date": "20261231"}