FDA.reportPublic FDA data

SAN X E2

Manufacturer
Amerisan, LLC | Best Sanitizers
Effective date
2024-12-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:44:03

Label at a glance#

ProductSAN X E2
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

handwash to help reduce bacteria that potentially can cause disease helps to prevent cross-contamination by hand contact helps to prevent drying of the skin recommended for repeated use

Dosage and administration

wet hands and wrists with clean, running water apply appropriate amount of product lather and scrub hands, fingers, fingernails, cuticles and wrists for at least 20 seconds rinse thoroughly with running water dry hands completely (incomplete drying may result in chapped skin)

Storage and handling

store in a cool, dry place below 104 F (40 C)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.12%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • handwash to help reduce bacteria that potentially can cause disease
  • helps to prevent cross-contamination by hand contact
  • helps to prevent drying of the skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this productdo not use in or near eyes.

OTC - STOP USE SECTION

Stop use and consult a doctor ifirritation and redness develop.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, seek medical attention or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands and wrists with clean, running water
  • apply appropriate amount of product
  • lather and scrub hands, fingers, fingernails, cuticles and wrists for at least 20 seconds
  • rinse thoroughly with running water
  • dry hands completely (incomplete drying may result in chapped skin)

Other information

STORAGE AND HANDLING SECTION

store in a cool, dry place below 104 F (40 C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, cocamidopropyl betaine, glycerine, polyethylene-polypropylene glycol, benzyl alcohol, phenoxyethanol, tetra sodium EDTA, dehydroacetic acid, sodium hydroxide, citric acid

Questions?

OTC - QUESTIONS SECTION

Contact Best Sanitizers at 888-225-3267Mon-Fri 9am - 4pm PST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SAN X

E2

Sanitizing

Foam

Soap

  • 0.12% Benzalkonium Chloride

(BZK) formula

  • Formulated with emollients

to help keep skin soft

  • Fragrance and Dye Free
  • Kosher, Pareve and Halal certified

NSF

Nonfood Compounds

Program Listed (E2)

Registration #

AMERISAN

Net Contents: 1250 mL (42.27 fl. oz)

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1053188benzalkonium chloride 0.12 % Medicated Liquid SoapPSN2
1053188benzalkonium chloride 1.2 MG/ML Medicated Liquid SoapSCD2
1053188benzalkonium chloride 0.12 % Medicated Liquid SoapSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69884-706-06SAN X E21250 mL in 1 BOTTLELIQUID12502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69884-706SAN X E2 (BENZALKONIUM CHLORIDE) LIQUID [AMERISAN, LLC]2Current NDC, Legacy NDC, 1 package rows20241218_d6e2f275-4609-24e6-e053-2995a90a8dd3.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69884-70669884-706-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
GLYCERINPDC6A3C0OXIACT
BENZYL ALCOHOLLKG8494WBHIACT
POLYETHYLENE GLYCOL 800UH6KR4953DIACT
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
EDETATE SODIUMMP1J8420LUIACT
DEHYDROACETIC ACID2KAG279R6RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
PHENOXYETHANOLHIE492ZZ3TIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
SAN X E2BENZALKONIUM CHLORIDEAmerisan, LLCd6e2f275-4609-24e6-e053-2995a90a8dd32024-12-16WarningsExact identifier
ndc (package): 69884-706-06
ndc (product): 69884-706
ndc11 (package): 69884070606
spl id: 2965dbef-0591-4303-e063-6394a90aeddc
spl set id: d6e2f275-4609-24e6-e053-2995a90a8dd3

Reported adverse events (FAERS/openFDA)#

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