ANTISEPTIC WIPE

Manufacturer
Diamond Wipes International
Effective date
2023-11-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:19:26

Label at a glance#

ProductANTISEPTIC WIPE
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

■ for hand sanitizing to decrease bacteria on skin when water and soap are not available ■ recommended for repeated use

Dosage and administration

■ tear open packet, remove wipe ■ wet hands thoroughly with product

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

■ for hand sanitizing to decrease bacteria on skin when water and soap are not available

■ recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

When using this product do not use in or near eyes. If contact occurs, flush thoroughly with water

Discontinue use if irritation or redness develops, if condition persists for more than 72 hours contact a doctor

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenIf swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

■ tear open packet, remove wipe ■ wet hands thoroughly with product

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Citric Acid, Fragrance, Glycerin,

Hamamelis Virginiana (Witch Hazel) Bark/Leaf/Twig Extract, Phenoxyethanol, Polysorbate

20, Potassium Sorbate, Sodium Benzoate, Tocopheryl Acetate, Water

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

*Escherichia coli, Staphylococcus aureus, Salmonella typhimurium, Pseudomonas aeruginosa, Burkholderia cepacia,
Enterobacter cloacae, Enterococcus faecalis, Streptococcus pyogenes, Candida albicans, Aspergillus brasiliensis

Vegan • Cruelty-Free
No added Gluten, Paraben, GMO, Sulfate, Phthalate, or Triclosan

©2022 Diamond Wipes International, Inc. All rights reserved.
Chino, CA 91710 Wipes123.com

800-454-1077

Do not flush Tear Open from Side

HAND SANITIZING WIPE

• 99.9% EFFECTIVE against most common germs*
• Non-drying alcohol-free formula with Aloe and Vitamin E

handy clean

MAKE IN U.S.A. with global components

Do Not Flush

Drug Facts
Active ingredient Purpose
Benzalkonium Chloride 0.13%........................................................................Antimicrobial
Uses
■ for hand sanitizing to decrease bacteria on skin when water and soap are not available
■ recommended for repeated use

Warnings
For external use only
When using this product
do not use in or near eyes. If contact occurs, flush thoroughly with water

Drug Facts (continued)

Discontinue use if irritation or redness develops, if condition persists for more than 72 hours
contact a doctor
Keep out of reach of children If swallowed, get medical help or contact a Poison Control
Center right away

Directions ■ tear open packet, remove wipe ■ wet hands thoroughly with product

Inactive ingredients Aloe Barbadensis Leaf Juice, Citric Acid, Fragrance, Glycerin,
Hamamelis Virginiana (Witch Hazel) Bark/Leaf/Twig Extract, Phenoxyethanol, Polysorbate
20, Potassium Sorbate, Sodium Benzoate, Tocopheryl Acetate, Water

LABELLABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64709-105-102022-02-15C16284748780-1d6a99b39-97c6-a426-e053-dadaa90af4c2HAND SANITIZING WIPE
64709-105-102022-01-28C16284748780-1d6a99b39-97c6-a426-e053-dadaa90af4c2HAND SANITIZING WIPE

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64709-105ANTISEPTIC WIPE (BENZALKONIUM CHLORIDE WIPE) CLOTH [DIAMOND WIPES INTERNATIONAL]4Legacy NDC20231202_b3485a6b-1d8d-cec1-e053-2a95a90a0ee5.zip

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
64709-10564709-105-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

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
4f986198-8955-aec0-e063-6294a90abebeb3485a6b-1d8d-cec1-e053-2a95a90a0ee52026-04-16WarningsExact identifier
spl set id: b3485a6b-1d8d-cec1-e053-2a95a90a0ee5

Reported adverse events (FAERS/openFDA)#

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