CSI E3 Hand Sanitizer

Manufacturer
Central Solutions Inc
Effective date
2024-12-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:41:29

Label at a glance#

ProductCSI E3 Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

An effective antimicrobial hand cleanser for topical application Recommended for repeated use Reduces transient microorganisms on intact skin Keep hands from drying out due to repeated uses

Dosage and administration

Wet hands thoroughly with product. Allow to dry without wiping. Use no water or towels

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

An effective antimicrobial hand cleanser for topical application

Recommended for repeated use

Reduces transient microorganisms on intact skin

Keep hands from drying out due to repeated uses

Warnings

WARNINGS SECTION

For External Use Only.

Flammable, keep away from fire or opem flame

OTC - WHEN USING SECTION

When using this product:

Avoid contact with eyes

In case of eye contact, flush with water for 15 minutes

OTC - STOP USE SECTION

Discontinue use and see a doctor if irritation occurs

Avoid contact with broken skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product.

Allow to dry without wiping.

Use no water or towels

Other information

OTHER SAFETY INFORMATION

Not tested on animals

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Glycerin

Questions?

OTC - QUESTIONS SECTION

Call 800-255-0262

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CSI

E3 Hand Sanitizer

For Hand Washing

to Decrease Bacteria

On The Skin

Net Contents:

18 oz (532 mL)

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62654-139-01CSI E3 Hand Sanitizer3785 mL in 1 BOTTLE, PLASTICLIQUID37852
62654-139-02CSI E3 Hand Sanitizer236 mL in 1 BOTTLE, PLASTICLIQUID2362
62654-139-37CSI E3 Hand Sanitizer532 mL in 1 BOTTLE, PLASTICLIQUID5322
62654-139-38CSI E3 Hand Sanitizer946 mL in 1 BOTTLE, PLASTICLIQUID9462
62654-139-94CSI E3 Hand Sanitizer208197 mL in 1 DRUMLIQUID2081972

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62654-139CSI E3 HAND SANITIZER (ALCOHOL) LIQUID [CENTRAL SOLUTIONS INC]2Current NDC, Legacy NDC, 5 package rows20241210_aa07bb62-ef07-99e4-e053-2995a90ae4a8.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62654-13962654-139-01, 62654-139-38, 62654-139-37, 62654-139-02, 62654-139-94

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
CSI E3 Hand SanitizerALCOHOLCentral Solutions Incaa07bb62-ef07-99e4-e053-2995a90ae4a82024-12-09WarningsExact identifier
ndc (package): 62654-139-38
ndc (package): 62654-139-37
ndc (package): 62654-139-94
ndc (package): 62654-139-02
ndc (package): 62654-139-01
ndc (product): 62654-139
ndc11 (package): 62654013938
ndc11 (package): 62654013937
ndc11 (package): 62654013901
ndc11 (package): 62654013902
ndc11 (package): 62654013994
spl id: 28d98d99-34b4-bece-e063-6294a90a5395
spl set id: aa07bb62-ef07-99e4-e053-2995a90ae4a8

Reported adverse events (FAERS/openFDA)#

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