zoviro
Generic: benzalkonium chloride
Labeler: zoviro, llcDrug Facts
Product Profile
Brand Name
zoviro
Generic Name
benzalkonium chloride
Labeler
zoviro, llc
Dosage Form
SWAB
Routes
Active Ingredients
benzalkonium chloride .13 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
83814-001
Product ID
83814-001_31459c6a-45c2-bb69-e063-6294a90a58dc
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2024-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83814001
Hyphenated Format
83814-001
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
zoviro (source: ndc)
Generic Name
benzalkonium chloride (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .13 g/100g
Packaging
- 20 POUCH in 1 BAG (83814-001-01) / 3.136 g in 1 POUCH
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "31459c6a-45c2-bb69-e063-6294a90a58dc", "openfda": {"upc": ["0383814000023"], "unii": ["F5UM2KM3W7"], "rxcui": ["1038558"], "spl_set_id": ["0b567ef2-a782-3daa-e063-6294a90a064e"], "manufacturer_name": ["Zoviro, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 POUCH in 1 BAG (83814-001-01) / 3.136 g in 1 POUCH", "package_ndc": "83814-001-01", "marketing_start_date": "20240301"}], "brand_name": "Zoviro", "product_id": "83814-001_31459c6a-45c2-bb69-e063-6294a90a58dc", "dosage_form": "SWAB", "product_ndc": "83814-001", "generic_name": "Benzalkonium Chloride", "labeler_name": "Zoviro, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zoviro", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".13 g/100g"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}