KISS MY FACE HAND SANITIZER WITH ALOE BACTERIAL DEFENSE FRAGRANCE FREE- benzalkonium chloride liquid 
Windmill Health Products, 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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Kiss My Face® Hand Sanitizer with Aloe Bacterial Defense Fragrance Free

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

Warnings

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Ask a doctor

Stop use and consult a doctor if irritation or redness develops. If condition persists for more than 72 hours, discontinue use.

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

Do not use on children less than 2 months of age or on open skin wounds

Directions

Apply a small amount of gel into palm of hand. Rub thoroughly over all surfaces of both hands for 15 seconds.

Other information

Store tightly closed, in a cool dry place.

Inactive ingredients

Water, Aloe Barbadensis Leaf Extract, Sodium Hyaluronate, Cocos Nucifera (Coconut) Oil, Gylcerin, Polyacrylamide, Tocopheryl Acetate, Propylene Glycol, Polyquaternium-7, Polysorbate 20, C13-14 Isoparaffin, Laureth-7, Phenoxyethanol, Aminomethyl Propanol

Questions or comments

1.800.822.4320

Made in the USA.

PRINCIPAL DISPLAY PANEL - 502 ML Bottle Label

KISS
MY
FACE®

HAND
SANITIZER
WITH ALOE

BACTERIAL DEFENSE

FRAGRANCE FREE

MOISTURIZING FORMULA
ANTIMICROBIAL ANTISEPTIC
ALCOHOL FREE | PARABEN FREE
17 FL OZ (502 ML)

310L0835001

Principal Display Panel - 502 ML Bottle Label
KISS MY FACE HAND SANITIZER WITH ALOE BACTERIAL DEFENSE FRAGRANCE FREE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74154-006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE130 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
COCONUT OIL (UNII: Q9L0O73W7L)  
GLYCERIN (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
LAURETH-7 (UNII: Z95S6G8201)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74154-006-17502 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/08/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333A05/08/2020
Labeler - Windmill Health Products, LLC (831136267)
Establishment
NameAddressID/FEIBusiness Operations
Cemi International015038336MANUFACTURE(74154-006)

Revised: 2/2022
Document Id: 9d067216-67b7-44f9-8df9-d8378e3c4ce2
Set id: dd645161-94d0-4b60-b470-273d57e2c68a
Version: 2
Effective Time: 20220204
 
Windmill Health Products, LLC