FDA.reportPublic FDA data

Wet Ones

Manufacturer
FOSHAN CITY SHUNDE AREA SOSHIO WET TISSUE CO., LTD.
Effective date
2017-08-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:12

Label at a glance#

ProductWet Ones Fresh Scent
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

adults and children ■ apply to hands 2 years and over ■ allow skin to dry without wiping children under 2 years ask a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.09%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

decreases bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

if you are allergic to any of the ingredients

When using this product

OTC - WHEN USING SECTION

do not get into eyes. If eye contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

if irritation or rash develops and continues for more than 72 hours.

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

adults and children ■ apply to hands

2 years and over ■ allow skin to dry without wiping

children under 2 years ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Alcohol Denat., Glycerin, Potassium Sorbate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Polysorbate 20, Fragrance, Citric Acid, Disodium Cocoamphodiacate, PEG-75 Lanolin, Sodium Chloride, Denatonium Benzoate

Questions or Comments?

OTC - QUESTIONS SECTION

Call 1-866-WET-111S; (1-866-938-1117), M-F

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130076828023743GTIN-13: 0076828023743
EAN-13: 0076828023743
GTIN-12: 076828023743
UPC-A: 076828023743
GTIN storage (14 digits): 00076828023743		Edgwlwpelbl.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
30493-001-102020-01-31C16284748780-19d75b9cf-dc16-f424-e053-dadaa90a57ceDrug Facts
30493-001-802020-01-31C16284748780-19d75b9cf-dc16-f424-e053-dadaa90a57ceDrug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30493-001WET ONES FRESH SCENT (BENZALKONIUM CHLORIDE) CLOTH [FOSHAN CITY SHUNDE AREA SOSHIO WET TISSUE CO., LTD.]1Legacy NDC20170814_56ba8688-6b74-5719-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30493-00130493-001-80, 30493-001-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
GLYCERINPDC6A3C0OXIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
POLYSORBATE 207T1F30V5YHIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
DENATONIUM BENZOATE4YK5Z54AT2IACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
PEG-75 LANOLIN09179OX7TBIACT
SODIUM CHLORIDE451W47IQ8XIACT

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
56ba8688-6b60-5719-e054-00144ff88e8856ba8688-6b74-5719-e054-00144ff88e882017-08-14WarningsExact identifier
spl id: 56ba8688-6b60-5719-e054-00144ff88e88
spl set id: 56ba8688-6b74-5719-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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