Alcohol Free Hand Sanitizer

Manufacturer
Guide Energy Solutions LLC
Effective date
2020-10-28
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:32:32

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.

Label contents#

Full prescribing information#

Active ingredient[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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Calcium Silicate

SPL UNCLASSIFIED SECTION

Kills 99.99% of Bacteria & Viruses

4-HR HAND SANITIZER

• NON-FLAMMABLE

• NON-TOXIC

• DYE FREE

• FRAGRANCE FREE

MADE IN THE USA

Manufactured By:

Guide Solutions
9330 S. Highway 99
Prague, OK 74864
405-567-0710

FDA Registered

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

PackagingPackaging

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN5
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD5
1049254benzalkonium chloride 0.13 % Topical SolutionSY5

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77042-110-01Alcohol Free Hand Sanitizer3785 mL in 1 JUGLIQUID37855
77042-110-02Alcohol Free Hand Sanitizer59 mL in 1 BOTTLELIQUID595
77042-110-16Alcohol Free Hand Sanitizer473 mL in 1 BOTTLELIQUID4735

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77042-110ALCOHOL FREE HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [GUIDE ENERGY SOLUTIONS LLC]5Legacy NDC, 3 package rows20201029_27171f80-1e8e-4a63-a61e-4fae937270b2.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
77042-11077042-110-02, 77042-110-16, 77042-110-01

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
14bfaf3b-0398-47b7-8d1a-7f895200589127171f80-1e8e-4a63-a61e-4fae937270b22020-10-28WarningsExact identifier
spl id: 14bfaf3b-0398-47b7-8d1a-7f8952005891
spl set id: 27171f80-1e8e-4a63-a61e-4fae937270b2

Reported adverse events (FAERS/openFDA)#

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