VIONEXUS

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: VIONEXUS
Generic name: ALCOHOL
Manufacturer: METREX RESEARCH, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 7542cf97-05fa-18e3-e053-2991aa0ac7eb
SPL ID: 508c3d3f-2ce1-2a3d-e063-6394a90aee9c
Version: 11
Effective date: 2026-04-28
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:08:31

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		VIONEXUS	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		METREX RESEARCH, LLC	openfda.manufacturer_name
ndc	package	55443-0400-2	openfda.package_ndc
ndc	package	55443-0400-5	openfda.package_ndc
ndc	package	55443-0400-7	openfda.package_ndc
ndc	package	55443-0400-4	openfda.package_ndc
ndc	package	55443-0400-3	openfda.package_ndc
ndc	package	55443-0400-6	openfda.package_ndc
ndc	package	55443-0400-1	openfda.package_ndc
ndc	product	55443-0400	openfda.product_ndc
ndc11	package	55443040007	derived:openfda.package_ndc
ndc11	package	55443040004	derived:openfda.package_ndc
ndc11	package	55443040001	derived:openfda.package_ndc
ndc11	package	55443040005	derived:openfda.package_ndc
ndc11	package	55443040002	derived:openfda.package_ndc
ndc11	package	55443040003	derived:openfda.package_ndc
ndc11	package	55443040006	derived:openfda.package_ndc
rxcui		1425407	openfda.rxcui
spl id		508c3d3f-2ce1-2a3d-e063-6394a90aee9c	id
spl set id		7542cf97-05fa-18e3-e053-2991aa0ac7eb	set_id
unii		3K9958V90M	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Flammable, keep away from fire or flame Do not ingest When using this product do not use in or near eyes discontinue use if irritation and redness develop Keep out of reach of children In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.