FDA.reportPublic FDA data

Pure Dew

Manufacturer
HOME & BODY COMPANY
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:17:23

Label at a glance#

ProductPure Dew
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Wash hands and rinse

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 hands

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

Wash hands and rinse

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Lauramine Oxide, Cellulose Gum, Tetrasodium EDTA, Polysorbate 20, Fragrance, Glycerin, Cocamidopropyl Betaine

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

64 front64 front64 back64 back16 front16 front16 back16 back

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
73746-03173746-031-01, 73746-031-02

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
POLYSORBATE 207T1F30V5YHIACT
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
EDETATE SODIUMMP1J8420LUIACT
WATER059QF0KO0RIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
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
ea614b18-c62e-fa11-e053-2a95a90a6279a70ce788-4bef-3e6d-e053-2995a90a2ee72022-10-06WarningsExact identifier
spl set id: a70ce788-4bef-3e6d-e053-2995a90a2ee7

Reported adverse events (FAERS/openFDA)#

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