ALCOHOL-FREE HAND SANITIZING FOAM- benzalkonium chloride solution 
United Laboratories Inc.

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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Alcohol-Free Hand Sanitizing Foam

Drug Facts

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

For external use only

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

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

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

Directions

Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Inactive ingredients

Water, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, citric acid and fragrance.

PRINCIPAL DISPLAY PANEL - 2 Ounce Bottle Label

UNITED
LABORATORIES

United 764

MICROMOUSSE

Alcohol-Free
Hand Sanitizing Foam

2 FLUID OUNCES

Eliminates 99.99% of common
disease-causing germs.

Made in USA
1018

UNITED LABORATORIES, INC.
320 37th Avenue • St. Charles, IL 60174
1-800-323-2594 • www.unitedlabsinc.com

PRINCIPAL DISPLAY PANEL - 2 Ounce Bottle Label
ALCOHOL-FREE HAND SANITIZING FOAM 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63998-764
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63998-764-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2019
2NDC:63998-764-02750 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E01/01/2019
Labeler - United Laboratories Inc. (001759737)
Establishment
NameAddressID/FEIBusiness Operations
Woodbine Products Company004220323MANUFACTURE(63998-764)

Revised: 11/2020
Document Id: 63f98a4a-af4d-4deb-a37e-6b3aad06c3bc
Set id: 4f5ddead-1868-45c2-9657-762c9ca3a0e2
Version: 1
Effective Time: 20201109
 
United Laboratories Inc.