swisher
Generic: benzalkonium chloride
Labeler: ecolab inc.Drug Facts
Product Profile
Brand Name
swisher
Generic Name
benzalkonium chloride
Labeler
ecolab inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
benzalkonium chloride 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
47593-591
Product ID
47593-591_842818aa-22c4-4bc6-b1c7-9978020a6923
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2018-06-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
47593591
Hyphenated Format
47593-591
Supplemental Identifiers
RxCUI
UPC
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
swisher (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 (47593-591-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "842818aa-22c4-4bc6-b1c7-9978020a6923", "openfda": {"upc": ["0025469040749"], "unii": ["F5UM2KM3W7"], "rxcui": ["1731737"], "spl_set_id": ["04e2f617-0643-4097-8780-b64c58c5b56c"], "manufacturer_name": ["Ecolab Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "750 mL in 1 BOTTLE, PLASTIC (47593-591-41)", "package_ndc": "47593-591-41", "marketing_start_date": "20180620"}], "brand_name": "Swisher", "product_id": "47593-591_842818aa-22c4-4bc6-b1c7-9978020a6923", "dosage_form": "SOLUTION", "product_ndc": "47593-591", "generic_name": "Benzalkonium Chloride", "labeler_name": "Ecolab Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Swisher", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "5 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180620", "listing_expiration_date": "20261231"}