MERINGUE FOAMING ANTIBACTERIAL HAND- 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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Drug Facts

Active ingredient

BENZALKONIUM CHLORIDE, 0.13%

Purpose

Antibacterial

Uses

for handwashing to reduce bacteria on the skin

Warnings

For external use only

When using this product

avoid contact with eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if

irritation and redness develop and persist for more than 3 days.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply foaming cleanser to dry hands
rub hands together to spread lather
wash for 15-20 seconds
rinse & dry hands thoroughly

Inactive ingredients

AQUA (WATER), GLYCERIN, LAURAMINE OXIDE, BUTYLENE GLYCOL, LACTIC ACID, SALICYLIC ACID, PARFUM (FRAGRANCE), GREEN 5 (CI 61570), YELLOW 5 (CI 19140).

57255-DCN9305 United Lab Meringue Antibac.jpg

UNITED LABORATORIES

United 758
MERINGUE
Foaming Antibacterial Hand Soap
PRECAUCION AL USARIO: Si usted no pede leer Ingles, pregunte a alguien que le traduzca esta etigueta para usted antes de uso.
A high-quality, foam soap that is 99.99% effective against common bacteria.
An SDS for this product is available through United’s website, www.unitedlabsinc.com, providing 24 hour access. Please read the SDS carefully and follow all directions when using or handling this product. Never reuse empty containers. Incompatible materials may adversely react.
NDC 63998-010-27
Manufactured in U.S.A.
1017
1 L (33.8 fl oz)

Sold By: UNITED LABORATORIES, INC.

320 37th Avenue ● St. Charles, IL 60174 ● 1-800-323-2594 ● www.unitedlabsinc.com

MERINGUE  FOAMING ANTIBACTERIAL HAND
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63998-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
LACTIC ACID (UNII: 33X04XA5AT)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63998-010-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/11/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/11/2018
Labeler - United Laboratories, Inc. (001759737)

Revised: 1/2018
Document Id: 812e0e87-b604-43e1-ba7a-70fd2cf8c42b
Set id: aac9a2f0-33b1-44c7-bb2c-41a42540ca70
Version: 1
Effective Time: 20180111
 
United Laboratories, Inc.