FDA.reportPublic FDA data

Wet Wipes

Manufacturer
Delta Brands, Inc
Effective date
2023-07-24
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 21:28:02

Label at a glance#

ProductWet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

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 contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

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 to dry

without wiping

children under ask a doctor

2 years before use

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, propylene glycol, cocamidopropyl betaine,PEG-7 glyceryl cocoate, fragrance, phenylmethanol, methylchloroisothiazolinine, methylisothiazolinone, PEG-40 hydrogenated castor oil, tetrasodium EDTA, cetrimonium chloride, citric acid, tocopherol acetate

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20276-43520276-435-30, 20276-435-40, 20276-435-16, 20276-435-80, 20276-435-60, 20276-435-12, 20276-435-36, 20276-435-35, 20276-435-42, 20276-435-50, 20276-435-24

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
EDETATE SODIUMMP1J8420LUIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
WATER059QF0KO0RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
01424913-54eb-2dbd-e063-6394a90ae0f7a64464a6-7c18-24e8-e053-2a95a90a9fbf2023-07-24WarningsExact identifier
spl id: 01424913-54eb-2dbd-e063-6394a90ae0f7
spl set id: a64464a6-7c18-24e8-e053-2a95a90a9fbf

Reported adverse events (FAERS/openFDA)#

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