VIROCIDE ANTIBACTERIAL WIPES- benzalkonium chloride, isopropyl alcohol cloth

Virocide Antibacterial Wipes by

Drug Labeling and Warnings

Virocide Antibacterial Wipes by is a Otc medication manufactured, distributed, or labeled by Virocide LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient
Benzalkonium Chloride 0.25%
Isopropyl Alcohol 5%

PURPOSE

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

INDICATIONS & USAGE

Uses decrease bacteria on skin.

WARNINGS

Warnings
For external use only.

WHEN USING

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

DO NOT USE

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

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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.

QUESTIONS

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

INACTIVE INGREDIENT

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

BOX OF 12-PACKETS

PACKET OF 100 WIPES

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INGREDIENTS AND APPEARANCE

VIROCIDE ANTIBACTERIAL WIPES 
benzalkonium chloride, isopropyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77005-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	2.5 mg
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	5 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
DIMETHICONE (UNII: 92RU3N3Y1O)
EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6)
HYDANTOIN (UNII: I6208298TA)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77005-007-02	12 in 1 BOX	10/07/2020
1	NDC: 77005-007-01	100 in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - Virocide LLC (117469716)

Registrant - Virocide LLC (117469716)