MERINGUE

Manufacturer
United Laboratories, Inc.
Effective date
2018-01-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:58

Label at a glance#

ProductMERINGUE Foaming Antibacterial Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

for handwashing to reduce bacteria on the skin

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE, 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for handwashing to reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

INSTRUCTIONS FOR USE SECTION

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

57255-DCN9305 United Lab Meringue Antibac.jpg57255-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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN1
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD1
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY1
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63998-010-272023-01-30C16284748780-1f386c64a-4633-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63998-010-27MERINGUEFoaming Antibacterial Hand1000 mL in 1 BOTTLE, PLASTICSOLUTION10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63998-010MERINGUE FOAMING ANTIBACTERIAL HAND (BENZALKONIUM CHLORIDE) SOLUTION [UNITED LABORATORIES, INC.]1Legacy NDC, 1 package rows20180617_aac9a2f0-33b1-44c7-bb2c-41a42540ca70.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63998-01063998-010-27

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
812e0e87-b604-43e1-ba7a-70fd2cf8c42baac9a2f0-33b1-44c7-bb2c-41a42540ca702018-01-11WarningsExact identifier
spl id: 812e0e87-b604-43e1-ba7a-70fd2cf8c42b
spl set id: aac9a2f0-33b1-44c7-bb2c-41a42540ca70

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.