zoviro

Generic: alcohol

Labeler: zoviro, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name zoviro
Generic Name alcohol
Labeler zoviro, llc
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

alcohol 70 mL/100mL

Manufacturer
Zoviro, LLC

Identifiers & Regulatory

Product NDC 83814-005
Product ID 83814-005_40844d7d-3a4d-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 2024-01-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83814005
Hyphenated Format 83814-005

Supplemental Identifiers

RxCUI
582753
UPC
0383814000085
UNII
3K9958V90M

Packaging Origin

Original Packager
true

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 alcohol (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 70 mL/100mL
source: ndc
Packaging
  • 60 mL in 1 BOTTLE (83814-005-01)
source: ndc

Packages (1)

83814-005-01 60 mL in 1 BOTTLE (83814-005-01)

Ingredients (1)

alcohol (70 mL/100mL)

Linked Drug Pages (1)

Zoviro ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "40844d7d-3a4d-ce94-e063-6294a90a7fa7", "openfda": {"upc": ["0383814000085"], "unii": ["3K9958V90M"], "rxcui": ["582753"], "spl_set_id": ["0e85fb58-7cca-8ae3-e063-6294a90a2553"], "manufacturer_name": ["Zoviro, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE (83814-005-01)", "package_ndc": "83814-005-01", "marketing_start_date": "20240109"}], "brand_name": "Zoviro", "product_id": "83814-005_40844d7d-3a4d-ce94-e063-6294a90a7fa7", "dosage_form": "LIQUID", "product_ndc": "83814-005", "generic_name": "ALCOHOL", "labeler_name": "Zoviro, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zoviro", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240109", "listing_expiration_date": "20261231"}