FDA.reportPublic FDA data

Virocide Antibacterial Wipes

Manufacturer
Virocide LLC
Effective date
2020-10-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:10

Label at a glance#

ProductVirocide Antibacterial Wipes
Active ingredientBENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL
Label structure14 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Benzalkonium Chloride 0.25%
Isopropyl Alcohol 5%

OTC - PURPOSE SECTION

Purpose
Benzalkonium Chloride .......................... Antimicrobial Agent
Isopropyl Alcohol ................................... Antimicrobial Agent

INDICATIONS & USAGE SECTION

Uses decrease bacteria on skin.

WARNINGS SECTION

Warnings
For external use only.

OTC - WHEN USING SECTION

When using this product, avoid contact with the eyes.
In case of contact, rinse eyes thoroughly with water.

OTC - DO NOT USE SECTION

Do not use if you are allergic to any of
the ingredients.

OTC - WHEN USING SECTION

When using this product do not get
into eyes. If contact occurs, rinse
thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation
or rash develops and continues for
more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If
swallowed get medical help or contact
a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions
adults and children   ■ apply to hands.
2 years and over:     ■ allow to dry
                                    without wiping.
children under 2 years: ask a doctor
before using.

OTC - QUESTIONS SECTION

Questions or Comments?
(M-F 9AM-5PM)
1(833)494-5459

INACTIVE INGREDIENT SECTION

Inactive Ingredients
Water, Aloe Vera (Aloe Barbadensis)
Leaf, Anhydrous Citric Acid,
Dimethicone, Edetate Sodium
Tetrahydrate, Hydantoin,
Polysorbate 20,Tocopheryl Acetate
(Vitamin E), Glycerin, Fragrance,
Methylchloroisothiazolinone,
Methylisothiazolinone.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BOX OF 12-PACKETS

77005-007 Box77005-007 Box

PACKET OF 100 WIPES

77005-007 Packet77005-007 Packet

res

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77005-007-022022-01-28C16284748780-1d6a99b39-fc18-a426-e053-dadaa90af4c2Virocide Antibacterial Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77005-007-01Virocide Antibacterial Wipes100 in 1 PACKETCLOTH1001
77005-007-02Virocide Antibacterial Wipes12 in 1 BOXCLOTH121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77005-007VIROCIDE ANTIBACTERIAL WIPES (BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL) CLOTH [VIROCIDE LLC]1Legacy NDC, 2 package rows20201008_136bc22a-8085-4d17-8b46-2bad85d5e06a.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77005-00777005-007-01, 77005-007-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ISOPROPYL ALCOHOLND2M416302ACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
DIMETHICONE92RU3N3Y1OIACT
EDETATE SODIUM TETRAHYDRATEL13NHD21X6IACT
HYDANTOINI6208298TAIACT
POLYSORBATE 207T1F30V5YHIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
766a7985-2857-4d46-bdc1-fcf692d026c7136bc22a-8085-4d17-8b46-2bad85d5e06a2020-10-07WarningsExact identifier
spl id: 766a7985-2857-4d46-bdc1-fcf692d026c7
spl set id: 136bc22a-8085-4d17-8b46-2bad85d5e06a

Reported adverse events (FAERS/openFDA)#

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