FDA.reportPublic FDA data

Antibacterial Hand Sanitizer

Manufacturer
Webb Business Promotions, Inc
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:46:20

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

Active Ingridient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride

Inactive Ingridients

INACTIVE INGREDIENT SECTION

Water, Aloe Vera, Glycerin, Propylene Glycol, Tocopherol

Purpose

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Warning

WARNINGS SECTION

Flammable

DOSAGE & ADMINISTRATION SECTION

Spray small ammount in your palm and briskly rub hands together until dry.

OTHER SAFETY INFORMATION

For external use only

INDICATIONS & USAGE SECTION

For external use only.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Non-Alcoholic Hand SanitizerNon-Alcoholic Hand SanitizerNON-ALCOHOLIC HAND SANITIZER

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70445-420-102023-07-28C16284748780-10191ceaa-6fcc-198a-e063-dbdaa90aec3eAntibacterial Hand Sanitizer
70445-420-372023-07-28C16284748780-10191ceaa-6fcc-198a-e063-dbdaa90aec3eAntibacterial Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70445-420-10Antibacterial Hand Sanitizer10 mL in 1 BOTTLESPRAY104
70445-420-37Antibacterial Hand Sanitizer3785 mL in 1 BOTTLESPRAY37854

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70445-420ANTIBACTERIAL HAND SANITIZER (NON-ALCOHOLIC HAND SANITIZER) SPRAY [WEBB BUSINESS PROMOTIONS, INC]4Legacy NDC, 2 package rows20220105_af6f96ac-a4fe-1f4e-e053-2a95a90a3fb1.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
70445-42070445-420-10, 70445-420-37

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
TOCOPHEROLR0ZB2556P8IACT
ALOE VERA LEAFZY81Z83H0XIACT

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
d4c7360f-8945-5b57-e053-2a95a90a7dbbaf6f96ac-a4fe-1f4e-e053-2a95a90a3fb12022-01-04WarningsExact identifier
spl id: d4c7360f-8945-5b57-e053-2a95a90a7dbb
spl set id: af6f96ac-a4fe-1f4e-e053-2a95a90a3fb1

Reported adverse events (FAERS/openFDA)#

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