antibacterial
Generic: benzalkonium chloride 0.13%
Labeler: ulineDrug Facts
Product Profile
Brand Name
antibacterial
Generic Name
benzalkonium chloride 0.13%
Labeler
uline
Dosage Form
SOAP
Routes
Active Ingredients
benzalkonium chloride 1.3 g/mL
Manufacturer
Identifiers & Regulatory
Product NDC
69790-279
Product ID
69790-279_4b0978d3-0a91-b165-e063-6294a90a7d7a
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2015-01-19
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69790279
Hyphenated Format
69790-279
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
antibacterial (source: ndc)
Generic Name
benzalkonium chloride 0.13% (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.3 g/mL
Packaging
- 221 mL in 1 BOTTLE, PUMP (69790-279-96)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4b0978d3-0a91-b165-e063-6294a90a7d7a", "openfda": {"unii": ["F5UM2KM3W7"], "spl_set_id": ["57c7bf8f-c17a-41b5-9b66-e4d16d6650a7"], "manufacturer_name": ["Uline"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "221 mL in 1 BOTTLE, PUMP (69790-279-96)", "package_ndc": "69790-279-96", "marketing_start_date": "20150119"}], "brand_name": "Antibacterial", "product_id": "69790-279_4b0978d3-0a91-b165-e063-6294a90a7d7a", "dosage_form": "SOAP", "product_ndc": "69790-279", "generic_name": "Benzalkonium chloride 0.13%", "labeler_name": "Uline", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antibacterial", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 g/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150119", "listing_expiration_date": "20271231"}