Protect U Guard Foaming Hand Sanitizer Alcohol Free

Manufacturer
Protect U Guard, LLC | Aire-Master of America, Inc
Effective date
2017-11-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:53

Label at a glance#

ProductProtect U Guard Foaming Hand Sanitizer Alcohol Free
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

Dispense an adequate amount in your palm to cover all surfaces of hands completely. Rub hnads together until dry. Supervise children in the use of this product.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and aska a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of chidren. If swallowed, get medical help or contacta a Poison Control Center right away.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

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 your palm to cover all surfaces of hands completely.

Rub hnads together until dry.

Supervise children in the use of this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocate, Citric Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

18 Ounce Label18 Ounce Label1000 ML Front1000 ML Front1000 ML Back1000 ML Back

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN1
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD1
1038799benzalkonium chloride 0.1 % Topical FoamSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130854654007201GTIN-13: 0854654007201
EAN-13: 0854654007201
GTIN-12: 854654007201
UPC-A: 854654007201
GTIN storage (14 digits): 00854654007201
Protect U Guard label proofs 2.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71788-234-202020-01-31C16284748780-19d75b9d0-c667-f424-e053-dadaa90a57ce5d2cc1f9-3b3d-7385-e053-2a91aa0a1279
71788-234-602020-01-31C16284748780-19d75b9d0-c667-f424-e053-dadaa90a57ce5d2cc1f9-3b3d-7385-e053-2a91aa0a1279

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71788-234-10Protect U Guard Foaming Hand Sanitizer Alcohol Free1000 mL in 1 BOTTLE, DISPENSINGLIQUID10001
71788-234-20Protect U Guard Foaming Hand Sanitizer Alcohol Free4 in 1 CARTONLIQUID41
71788-234-50Protect U Guard Foaming Hand Sanitizer Alcohol Free530 mL in 1 BOTTLELIQUID5301
71788-234-60Protect U Guard Foaming Hand Sanitizer Alcohol Free6 in 1 CARTONLIQUID61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71788-234PROTECT U GUARD FOAMING HAND SANITIZER ALCOHOL FREE (BENZALKONIUM CHLORIDE) LIQUID [PROTECT U GUARD, LLC]1Legacy NDC, 4 package rows20171106_5d2cc1f9-3b3d-7385-e053-2a91aa0a1279.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71788-23471788-234-50, 71788-234-60, 71788-234-10, 71788-234-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
5d2cc1f9-3b3e-7385-e053-2a91aa0a12795d2cc1f9-3b3d-7385-e053-2a91aa0a12792017-11-06WarningsExact identifier
spl id: 5d2cc1f9-3b3e-7385-e053-2a91aa0a1279
spl set id: 5d2cc1f9-3b3d-7385-e053-2a91aa0a1279

Reported adverse events (FAERS/openFDA)#

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