FDA.reportPublic FDA data

ALPET QE2 SANITIZING FOAM

Product NDC
59900-214
11-digit product format
599000214
Labeler code
59900
Product ID
59900-214_288e37ae-012f-23f8-e063-6394a90a586b
Type
HUMAN OTC DRUG
Nonproprietary name
BENZALKONIUM CHLORIDE
Dosage form
LIQUID
Route
TOPICAL
Labeler
Best Sanitizers, Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-05-03
Substance
BENZALKONIUM CHLORIDE
Active strength
1.2 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
ALPET QE2 SANITIZING FOAM
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE1.2 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
1053188Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
0aa71f9d-f660-4a32-b54a-1968aea9d0eeAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59900-214-01ALPET QE2 SANITIZING FOAM946352 mL in 1 TANKLIQUID9463522
59900-214-02ALPET QE2 SANITIZING FOAM208197 mL in 1 DRUMLIQUID2081972
59900-214-03ALPET QE2 SANITIZING FOAM3785 mL in 1 JUGLIQUID37852
59900-214-05ALPET QE2 SANITIZING FOAM1250 mL in 1 BOTTLELIQUID12502
59900-214-08ALPET QE2 SANITIZING FOAM250 mL in 1 BOTTLELIQUID2502
59900-214-10ALPET QE2 SANITIZING FOAM59 mL in 1 BOTTLELIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59900-214ALPET QE2 SANITIZING FOAM (BENZALKONIUM CHLORIDE) LIQUID [BEST SANITIZERS, INC.]2Current NDC, Legacy NDC, 6 package rows20241222_0aa71f9d-f660-4a32-b54a-1968aea9d0ee.zip

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
ALPET QE2 SANITIZING FOAMBENZALKONIUM CHLORIDEBest Sanitizers, Inc.0aa71f9d-f660-4a32-b54a-1968aea9d0ee2024-12-05WarningsExact identifier
ndc (product): 59900-214

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1053188benzalkonium chloride 0.12 % Medicated Liquid SoapPSN0aa71f9d-f660-4a32-b54a-1968aea9d0ee2
1053188benzalkonium chloride 1.2 MG/ML Medicated Liquid SoapSCD0aa71f9d-f660-4a32-b54a-1968aea9d0ee2
1053188benzalkonium chloride 0.12 % Medicated Liquid SoapSY0aa71f9d-f660-4a32-b54a-1968aea9d0ee2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59900-214-0159900021401946352 mL in 1 TANK (59900-214-01) 946352 ml2019-05-030000-00-00NoNoCurrent
59900-214-0259900021402208197 mL in 1 DRUM (59900-214-02) 208197 ml2019-05-030000-00-00NoNoCurrent
59900-214-03599000214033785 mL in 1 JUG (59900-214-03) 3785 ml2019-05-030000-00-00NoNoCurrent
59900-214-05599000214051250 mL in 1 BOTTLE (59900-214-05) 1250 ml2019-05-030000-00-00NoNoCurrent
59900-214-0859900021408250 mL in 1 BOTTLE (59900-214-08) 250 ml2019-05-030000-00-00NoNoCurrent
59900-214-105990002141059 mL in 1 BOTTLE (59900-214-10) 59 ml2019-05-030000-00-00NoNoCurrent