VYTIS SHIELD ALOE VERA FOAM HAND SANITIZER- benzalkonium chloride spray 
Vytis Shield, Llc

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Vytis Shield Aloe Vera Foam - Hand Sanitizer

Drug Facts

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic Hand Sanitizer

Uses

Hand Sanitizer to help decrease bacteria on the skin.

Warnings

For external use only.

Do not use

in ears or mouth.

When using this product

avoid contact with the eyes.

  • In case of contact flush eyes with water.

Stop use and ask a doctor

if redness or irritation develops and persists for more than 72 hours.

Keep out of reach of children.

Children should be supervised when using this product. Do not freeze.

Directions

Apply a small amount into palms of hands and spread on both hands. Rub into skin until dry.

Inactive Ingredients

1-Octadecanaminium NN dimethyl (3-trimethoxysilyl) propyl chloride, Aloe Barbadenis leaf extract, C12-C15 Pareth 12, Caprylyl Glucoside, Citric Acid Monohydrate, Citronellol, FD&C Blue 1, Glycerin, Polyaminopropyl biguanide, Sodium benzoate, Water

Questions or comments

Call:1-888-489-2719

Mon. - Fri. 9:00 AM to 5:00 PM (EST)

Package Labeling:

Box

VYTIS SHIELD ALOE VERA FOAM HAND SANITIZER 
benzalkonium chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70299-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYAMINOPROPYL BIGUANIDE (UNII: 322U039GMF)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70299-001-001 in 1 BOX12/03/2015
150 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:70299-001-011 in 1 BOX12/03/2015
2236 mL in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:70299-001-021 in 1 BOX12/03/2015
31000 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)12/03/2015
Labeler - Vytis Shield, Llc (039382748)

Revised: 11/2023
Document Id: 09c28e4c-ceb0-8f33-e063-6294a90a580e
Set id: 7981633d-afc5-4bc1-9c2b-76c1a7b4c486
Version: 4
Effective Time: 20231109
 
Vytis Shield, Llc