Protect U Guard Antibacterial Foaming

Manufacturer
Protect U Guard, LLC | Whisk Products Inc
Effective date
2020-06-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:16:08

Label at a glance#

ProductProtect U Guard Antibacterial Foaming
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Apply a palmful to hands and forearms. Scrub thoroughly for at least fifteen seconds Rinse completely and dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Skin Antimicrobial

Use

INDICATIONS & USAGE SECTION

Reduces amount of bacteria on hands

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 Ask a Doctor of irritation or redness develops, or if condition persists for more than 72 hours.

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

For external use only

OTC - WHEN USING SECTION

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

Apply a palmful to hands and forearms.

Scrub thoroughly for at least fifteen seconds

Rinse completely and dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN2
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD2
1038799benzalkonium chloride 0.1 % Topical FoamSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71788-001-202023-01-30C16284748780-1f386c64a-0285-0266-e053-dadaa90a7c1aa735bf12-36f8-89b4-e053-2995a90a563e
71788-001-602023-01-30C16284748780-1f386c64a-0285-0266-e053-dadaa90a7c1aa735bf12-36f8-89b4-e053-2995a90a563e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71788-001-10Protect U Guard Antibacterial Foaming1000 mL in 1 BOTTLE, DISPENSINGLIQUID10002
71788-001-20Protect U Guard Antibacterial Foaming4 in 1 CARTONLIQUID42
71788-001-50Protect U Guard Antibacterial Foaming530 mL in 1 BOTTLELIQUID5302
71788-001-60Protect U Guard Antibacterial Foaming12 in 1 CARTONLIQUID122

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71788-001PROTECT U GUARD ANTIBACTERIAL FOAMING (BENZALKONIUM CHLORIDE) LIQUID [PROTECT U GUARD, LLC]2Legacy NDC, 4 package rows20200605_a735bf12-36f8-89b4-e053-2995a90a563e.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71788-00171788-001-50, 71788-001-60, 71788-001-10, 71788-001-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a7489d1b-0564-ee1a-e053-2995a90a4d87a735bf12-36f8-89b4-e053-2995a90a563e2020-06-04WarningsExact identifier
spl id: a7489d1b-0564-ee1a-e053-2995a90a4d87
spl set id: a735bf12-36f8-89b4-e053-2995a90a563e

Reported adverse events (FAERS/openFDA)#

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