finipil lait 50
Generic: benzethonium chloride
Labeler: equibal, inc.Drug Facts
Product Profile
Brand Name
finipil lait 50
Generic Name
benzethonium chloride
Labeler
equibal, inc.
Dosage Form
CREAM
Routes
Active Ingredients
benzethonium chloride 195 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
53228-050
Product ID
53228-050_461f32f5-973b-7cf2-e063-6294a90a254b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2013-03-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53228050
Hyphenated Format
53228-050
Supplemental Identifiers
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
finipil lait 50 (source: ndc)
Generic Name
benzethonium chloride (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 195 mg/100mL
Packaging
- 44 mL in 1 TUBE (53228-050-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "461f32f5-973b-7cf2-e063-6294a90a254b", "openfda": {"unii": ["PH41D05744"], "spl_set_id": ["bc630fbc-e428-4d46-8330-fb6f699943fd"], "manufacturer_name": ["Equibal, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "44 mL in 1 TUBE (53228-050-01)", "package_ndc": "53228-050-01", "marketing_start_date": "20130301"}], "brand_name": "finipil Lait 50", "product_id": "53228-050_461f32f5-973b-7cf2-e063-6294a90a254b", "dosage_form": "CREAM", "product_ndc": "53228-050", "generic_name": "BENZETHONIUM CHLORIDE", "labeler_name": "Equibal, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "finipil Lait 50", "active_ingredients": [{"name": "BENZETHONIUM CHLORIDE", "strength": "195 mg/100mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130301", "listing_expiration_date": "20261231"}