FDA.reportPublic FDA data

Personal CARE

Manufacturer
Delta Brands & Products LLC
Effective date
2018-04-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:59:58

Label at a glance#

ProductPersonal CARE FOAMING HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

■ for washing hands to decrease bacteria on the skin ■ recommended for repeated use.

Dosage and administration

■ wet hands thoroughly with product and rub into skin until dry ■ for children under 6, use only under adult supervision ■ not recommended for infants ■ no rinsing required.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ for washing hands to decrease bacteria on the skin ■ recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes. If contact occurs, flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash develops

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ wet hands thoroughly with product and rub into skin until dry ■ for children under 6, use only under adult supervision ■ not recommended for infants ■ no rinsing required.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water (aqua), disodium cocoamphodiacetate, glycerin, cetrimonium chloride, tetrasodium EDTA, fragrance, dimethicone, citric acid

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72133-149-072021-07-23C16284748780-1c7ccaba7-27c9-fd44-e053-dadaa90aa01bDrug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72133-149PERSONAL CARE FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [DELTA BRANDS & PRODUCTS LLC]2Legacy NDC20180413_69abe1b1-3aae-d8c2-e053-2a91aa0ab89f.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72133-14972133-149-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
DIMETHICONE92RU3N3Y1OIACT
EDETATE SODIUM TETRAHYDRATEL13NHD21X6IACT
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT

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
69ae73bf-c85b-53a2-e053-2991aa0ae18a69abe1b1-3aae-d8c2-e053-2a91aa0ab89f2018-04-12WarningsExact identifier
spl id: 69ae73bf-c85b-53a2-e053-2991aa0ae18a
spl set id: 69abe1b1-3aae-d8c2-e053-2a91aa0ab89f

Reported adverse events (FAERS/openFDA)#

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