FDA.reportPublic FDA data

Individual Free and Clear Foaming Antibacterial Skin Cleanser

Manufacturer
Brady Industries Inc. | Betco Corporation
Effective date
2022-03-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:48:44

Label at a glance#

ProductIndividual Free and Clear Foaming Antibacterial Skin Cleanser
Active ingredientDEHYDRATED ALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizer to reduce microorganisms on the skin. Use this product when soap and water are not available.

Dosage and administration

Read entire label before using this product. Place a palmful (5 grams) of product in one hand. Spread on both handsand rub into the skin until dry (1-2 min).

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to reduce microorganisms on the skin.

Use this product when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. FLAMMABLE. This product contains ethyl alcohol.

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs.

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

Directions

DOSAGE & ADMINISTRATION SECTION

Read entire label before using this product.

Place a palmful (5 grams) of product in one hand.

Spread on both handsand rub into the skin until dry (1-2 min).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, D&C Green #5, Fragrance, PEG-10 Acrylate/Perfluorohexylethyl Acrylate Copolymer, Perfluorohexylethyl Alcohol, Propylene Glycol, Water

Purpose

OTC - PURPOSE SECTION

Antiseptic

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Foaming Hand SanitizerFoaming Hand Sanitizer

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79258-795-292025-01-30C16284748780-12cef2736-6231-d83d-e063-dadaa90ab31fFoaming Hand Sanitizer

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79258-795INDIVIDUAL FREE AND CLEAR FOAMING ANTIBACTERIAL SKIN CLEANSER (BENZALKONIUM CHLORIDE) SOAP [BRADY INDUSTRIES INC.]1Legacy NDC20220315_da33a6ff-92f3-942f-e053-2995a90aa0db.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79258-79579258-795-29

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMERD76Z87928NIACT
D&C GREEN NO. 58J6RDU8L9XIACT
2-(PERFLUOROHEXYL)ETHANOLG2R5YO5N3VIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DEHYDRATED 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
41d55a6b-127f-b63f-e063-6294a90ab9d3da33a6ff-92f3-942f-e053-2995a90aa0db2025-10-23WarningsExact identifier
spl set id: da33a6ff-92f3-942f-e053-2995a90aa0db

Reported adverse events (FAERS/openFDA)#

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