bzk
Generic: benzalkonium chloride
Labeler: jianerkang medical co., ltdDrug Facts
Product Profile
Brand Name
bzk
Generic Name
benzalkonium chloride
Labeler
jianerkang medical co., ltd
Dosage Form
SWAB
Routes
Active Ingredients
benzalkonium chloride 1.33 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
34645-5008
Product ID
34645-5008_085c7bca-1ee1-9d63-e063-6294a90a6e18
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2006-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
346455008
Hyphenated Format
34645-5008
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
- 1.33 mg/mL
Packaging
- 1.4 mL in 1 POUCH (34645-5008-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "085c7bca-1ee1-9d63-e063-6294a90a6e18", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1043307"], "spl_set_id": ["d96c6ad2-c7e9-4079-9db2-59d108f284bb"], "manufacturer_name": ["Jianerkang Medical Co., Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1.4 mL in 1 POUCH (34645-5008-3)", "package_ndc": "34645-5008-3", "marketing_start_date": "20060101"}], "brand_name": "BZK", "product_id": "34645-5008_085c7bca-1ee1-9d63-e063-6294a90a6e18", "dosage_form": "SWAB", "product_ndc": "34645-5008", "generic_name": "Benzalkonium Chloride", "labeler_name": "Jianerkang Medical Co., Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BZK", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.33 mg/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20060101", "listing_expiration_date": "20261231"}