zoviro
Generic: benzalkonium chloride
Labeler: zoviro, llcDrug Facts
Product Profile
Brand Name
zoviro
Generic Name
benzalkonium chloride
Labeler
zoviro, llc
Dosage Form
LIQUID
Routes
Active Ingredients
benzalkonium chloride .12 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
83814-006
Product ID
83814-006_40844d7d-3a50-ce94-e063-6294a90a7fa7
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2025-04-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83814006
Hyphenated Format
83814-006
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
- .12 g/100mL
Packaging
- 281 mL in 1 BOTTLE, PUMP (83814-006-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "40844d7d-3a50-ce94-e063-6294a90a7fa7", "openfda": {"upc": ["0383814000245"], "unii": ["F5UM2KM3W7"], "rxcui": ["1046310"], "spl_set_id": ["33e1e96d-1058-35d5-e063-6394a90a4c9e"], "manufacturer_name": ["Zoviro, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "281 mL in 1 BOTTLE, PUMP (83814-006-01)", "package_ndc": "83814-006-01", "marketing_start_date": "20250421"}], "brand_name": "Zoviro", "product_id": "83814-006_40844d7d-3a50-ce94-e063-6294a90a7fa7", "dosage_form": "LIQUID", "product_ndc": "83814-006", "generic_name": "BENZALKONIUM CHLORIDE", "labeler_name": "Zoviro, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zoviro", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".12 g/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250421", "listing_expiration_date": "20261231"}