Alcohol Free Hand Sanitizer

Manufacturer
Devbond Consulting, L.l.c
Effective date
2021-04-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:39:33

Label at a glance#

ProductAlcohol Free Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

Dispense an adequate amount in palm to cover hands.  Rub hands together to cover skin thoroughly until dry. Supervise young children while using this product.

Storage and handling

*Skin cells may be shed naturally or by abrasion prior to 4 hours, exposing fresh, unprotected skin. Reapply as needed. Do not allow product to freeze.

Label contents#

Full prescribing information#

Active ingredients[s]

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Skin Antiseptic

Use[s]

INDICATIONS & USAGE SECTION

For hand and skin sanitizing to decrease microbes on skin.

Warnings

WARNINGS SECTION

For external use only. Do not use in the eyes. In case of eye contact, flush thoroughly with water & seek medical attention.

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

Dispense an adequate amount in palm to cover hands. 

Rub hands together to cover skin thoroughly until dry.

Supervise young children while using this product.

Other information

STORAGE AND HANDLING SECTION

*Skin cells may be shed naturally or by abrasion prior to 4 hours, exposing fresh, unprotected skin. Reapply as needed. Do not allow product to freeze.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Calcium Silicate

SPL UNCLASSIFIED SECTION

Kills 99.99% of Bacteria & Viruses

By DevbondUSA

4-HOUR HAND SANITIZER

NON-FLAMMABLE

NON-TOXIC

DYE FREE

FRAGRANCE FREE

UltraNanoClean Hand Sanitizer has proven residual antimicrobial benefits for up to four hours. It's active ingredient is a preferred skin antiseptic that kills germs on contacts and inhibits future microbial growth. In addition, the proprietary mineral blend enhances product bonding and long lasting effectiveness.

• Kills 99.9% of illness-causing germs on contact & persists on skin for up to 4 hours

• Alcohol Free,  Foaming Formula won't dry hands, sting or cause cracking

• Moisture-infused foam leaves skin feeling nourished & silky, even after repeated applications

• Outperforms alcohol-based sanitizers by persisting on skin; guarding against exposure

MADE IN THE USA

Distributed by:

DevBond USA

1836 Augusta Drive

Suite 16

Houston TX 77057

(713) 256-6160

FOR EXTERNAL USE ONLY

FDA Registered

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackagingPackagingPackagingPackagingPackagingPackagingPackagingPackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN3
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD3
1049254benzalkonium chloride 0.13 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79993-110-01Alcohol Free Hand Sanitizer3785 mL in 1 JUGLIQUID37853
79993-110-02Alcohol Free Hand Sanitizer59 mL in 1 BOTTLELIQUID593
79993-110-05Alcohol Free Hand Sanitizer18927 mL in 1 PAILLIQUID189273
79993-110-16Alcohol Free Hand Sanitizer473 mL in 1 BOTTLELIQUID4733

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79993-110ALCOHOL FREE HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [DEVBOND CONSULTING, L.L.C]3Legacy NDC, 4 package rows20210410_f034acda-b86e-441e-8c4f-1e2d48f2e0db.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79993-11079993-110-02, 79993-110-16, 79993-110-01, 79993-110-05

Ingredients#

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

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

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
5cd3f56e-c060-42fd-9fc6-0e858ea300a0f034acda-b86e-441e-8c4f-1e2d48f2e0db2021-04-05WarningsExact identifier
spl id: 5cd3f56e-c060-42fd-9fc6-0e858ea300a0
spl set id: f034acda-b86e-441e-8c4f-1e2d48f2e0db

Reported adverse events (FAERS/openFDA)#

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