FDA.reportPublic FDA data

Lavex Foaming Antibacterial Hand

Manufacturer
Clark Core Services, LLC
Effective date
2025-02-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:54:35

Label at a glance#

ProductLavex Foaming Antibacterial Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Apply a palmful to hands and forearms. Scrub thoroughly for at least fifteen seconds. Rinse completely and dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Skin Antimicrobial

Use

INDICATIONS & USAGE SECTION

Reduces amount of bacteria on hands

Warnings

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply a palmful to hands and forearms.
  • Scrub thoroughly for at least fifteen seconds.
  • Rinse completely and dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, DMDM Hydantoin, Citric Acid, Fragrance, Yellow 5, Red 40

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Case Label - 6 x 1000 mL BagsCase Label - 6 x 1000 mL Bags

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapPSN1
1233282benzalkonium chloride 1 MG/ML Medicated Liquid SoapSCD1
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81551-387-01Lavex Foaming Antibacterial Hand1000 mL in 1 BAGSOLUTION10001
81551-387-01Lavex Foaming Antibacterial Hand6 in 1 BAGSOLUTION61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81551-387LAVEX FOAMING ANTIBACTERIAL HAND (BENZALKONIUM CHLORIDE) SOLUTION [CLARK CORE SERVICES, LLC]1Current NDC, 2 package rows20250209_2d7d57dc-c3af-0fa8-e063-6394a90a00a0.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
81551-38781551-387-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
DMDM HYDANTOINBYR0546TOWIACT
FD&C RED NO. 40WZB9127XOAIACT
WATER059QF0KO0RIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

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
Lavex Foaming Antibacterial HandBENZALKONIUM CHLORIDEClark Core Services, LLC2d7d57dc-c3af-0fa8-e063-6394a90a00a02025-02-05WarningsExact identifier
ndc (package): 81551-387-01
ndc (product): 81551-387
ndc11 (package): 81551038701
spl id: 2d7d60da-6779-e443-e063-6294a90a792c
spl set id: 2d7d57dc-c3af-0fa8-e063-6394a90a00a0

Reported adverse events (FAERS/openFDA)#

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