bzk
Generic: benzalkonium chloride
Labeler: henry schein inc.Drug Facts
Product Profile
Brand Name
bzk
Generic Name
benzalkonium chloride
Labeler
henry schein inc.
Dosage Form
LIQUID
Routes
Active Ingredients
benzalkonium chloride .0013 g/g
Manufacturer
Identifiers & Regulatory
Product NDC
0404-6735
Product ID
0404-6735_1522e337-1394-24fa-e063-6394a90ae000
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2013-01-07
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04046735
Hyphenated Format
0404-6735
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
bzk (source: ndc)
Generic Name
benzalkonium chloride (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .0013 g/g
Packaging
- 100 PACKET in 1 BOX (0404-6735-01) / 2.5 g in 1 PACKET
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1522e337-1394-24fa-e063-6394a90ae000", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1038558"], "spl_set_id": ["ff877b63-fa58-4770-a882-694eda33203b"], "manufacturer_name": ["Henry Schein Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 PACKET in 1 BOX (0404-6735-01) / 2.5 g in 1 PACKET", "package_ndc": "0404-6735-01", "marketing_start_date": "20161201"}], "brand_name": "BZK", "product_id": "0404-6735_1522e337-1394-24fa-e063-6394a90ae000", "dosage_form": "LIQUID", "product_ndc": "0404-6735", "generic_name": "benzalkonium chloride", "labeler_name": "Henry Schein Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BZK", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".0013 g/g"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130107", "listing_expiration_date": "20261231"}