VIROCIDE ANTIBACTERIAL WIPES- benzalkonium chloride, isopropyl alcohol cloth 
Virocide LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Virocide Antibacterial Wipes

Drug Facts

Active ingredient
Benzalkonium Chloride 0.25%
Isopropyl Alcohol 5%

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

Uses decrease bacteria on skin.

Warnings
For external use only.

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

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

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

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

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

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

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

77005-007 Box

PACKET OF 100 WIPES

77005-007 Packet

res

VIROCIDE ANTIBACTERIAL WIPES 
benzalkonium chloride, isopropyl alcohol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77005-007
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE2.5 mg
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL5 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77005-007-0212 in 1 BOX10/07/2020
1NDC:77005-007-01100 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/30/2020
Labeler - Virocide LLC (117469716)
Registrant - Virocide LLC (117469716)

Revised: 10/2020
Document Id: 766a7985-2857-4d46-bdc1-fcf692d026c7
Set id: 136bc22a-8085-4d17-8b46-2bad85d5e06a
Version: 1
Effective Time: 20201007
 
Virocide LLC