FDA.reportPublic FDA data

Lavex Foaming Antibacterial Hand

Product NDC
81551-387
Requested package NDC
81551-387-01
11-digit product format
815510387
Labeler code
81551
Product ID
81551-387_2d7d60da-6779-e443-e063-6294a90a792c
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Clark Core Services, LLC
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-02-05
Substance
BENZALKONIUM CHLORIDE
Active strength
1 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated 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

Additional Listing Data#

Finished product
Yes
Brand name base
Lavex Foaming Antibacterial Hand
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE1 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F5UM2KM3W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1233282Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2d7d57dc-c3af-0fa8-e063-6394a90a00a0Available on FDA.report

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapPSN2d7d57dc-c3af-0fa8-e063-6394a90a00a01
1233282benzalkonium chloride 1 MG/ML Medicated Liquid SoapSCD2d7d57dc-c3af-0fa8-e063-6394a90a00a01
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapSY2d7d57dc-c3af-0fa8-e063-6394a90a00a01

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
81551-387-01815510387016 BAG in 1 BAG (81551-387-01) / 1000 mL in 1 BAG6 bag2025-02-05NoNoCurrent