FDA.reportPublic FDA data

Pure Dew Hand Sanitizer

Manufacturer
HOME & BODY COMPANY
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:17:36

Label at a glance#

ProductPure Dew Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Place enough product in your palm to throughly cover hands. Rub hands together briskly until dry

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

0.13% Benzalkonium Chloride

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Helps reduce bacterial on the skin

Warning

WARNINGS SECTION

For external use only.
When using this product do not use in or near the eyes.
In case of contact, rinse eyes throughly with water.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INSTRUCTIONS FOR USE SECTION

Place enough product in your palm to throughly cover hands. Rub hands together briskly until dry

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Fragrance, Glycerin, Isopropyl Alcohol, Polysorbate 20, Water (Aqua)

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
73746-04573746-045-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
POLYSORBATE 207T1F30V5YHIACT

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
ea61cc9e-6ed0-3b50-e053-2995a90a1826b1041f56-4dd8-99b5-e053-2995a90a35832022-10-06WarningsExact identifier
spl set id: b1041f56-4dd8-99b5-e053-2995a90a3583

Reported adverse events (FAERS/openFDA)#

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