MERINGUE FOAMING ANTIBACTERIAL HAND- benzalkonium chloride solution

MERINGUE by

Drug Labeling and Warnings

MERINGUE by is a Otc medication manufactured, distributed, or labeled by United Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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).

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

MERINGUE  FOAMING ANTIBACTERIAL HAND
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63998-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63998-010-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/11/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/11/2018

Labeler - United Laboratories, Inc. (001759737)