Redi Wipes

Manufacturer
Radienz Living, LLC
Effective date
2021-04-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:39:47

Label at a glance#

ProductRedi Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

To use, peel back label, pull out wipe and firmly reseal label to maintain package moisture. Do not remove label. Unfold cloth and rub thoroughly over all surfaces of both hands. Use only once and throw away. After cleansing, dispose of wipe in a trash receptacle. Rub hands together briskly to dry.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benalkonium chloride (0.115%)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Do Not Use

OTC - DO NOT USE SECTION

Do not use over large areas of the body or if you are allergic to any of these ingredients.

When using this product 

OTC - WHEN USING SECTION

Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

If irritation or redness develops and persists 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

  • To use, peel back label, pull out wipe and firmly reseal label to maintain package moisture. Do not remove label.
  • Unfold cloth and rub thoroughly over all surfaces of both hands. Use only once and throw away. After cleansing, dispose of wipe in a trash receptacle. Rub hands together briskly to dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Behentrimonium Chloride, Dihydroxypropyl Peg-5 Linoleammonium Chloride, Glycereth-2 Cocoate, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate (Vitamin E), Phenoxyethanol, Potassium Sorbate, Fragrance

Other Information

SPL UNCLASSIFIED SECTION

*Kills 99.9% of germs that may cause illness, including E. Coli and MRSA in just 15 seconds.

RediWipes logo™, Free Of logo™, and Wind Energy/Artesian Glacial Aquifer Water logo™ are trademarks of U.S. Nonwovens Corp.
All rights reserved.


**This product is not manufactured or distributed by Edgewell Personal Care, owner of the registered trademark, Wet Ones®.


DISTRIBUTED BY: U.S. NONWOVENS CORP. 100 EMJAY BLVD., BRENTWOOD, NY 11717

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SANITIZING REDI WIPESTM

Compare to Wet Ones®**

ANTIBACTERIAL HAND WIPES

FRESH SCENT

ALCOHOL FREE

KILLS 99.9% OF GERMS*

15 Soft Wipes

7 IN x 6 IN

(17.78 cm x 15.24 cm)

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049374benzalkonium Cl 0.115 % Medicated PadPSN2
1049374benzalkonium chloride 1.15 MG/ML Medicated PadSCD2
1049374benzalkonium chloride 0.115 % Medicated PadSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52553-004-152023-01-30C16284748780-1f386c64a-0b44-0266-e053-dadaa90a7c1aRedi Wipes Antibacterial Hand Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52553-004-15Redi Wipes15 in 1 PACKAGEPATCH152
52553-004-15Redi Wipes0.115 mg in 1 PATCHPATCH0.1152

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52553-004REDI WIPES (BENZALKONIUM CHLORIDE) PATCH [RADIENZ LIVING, LLC]2Legacy NDC, 2 package rows20210420_732ed952-8b99-4756-874d-6211a651d005.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52553-00452553-004-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
6626e154-7292-4e59-a55e-93dbcc3f662b732ed952-8b99-4756-874d-6211a651d0052021-04-19WarningsExact identifier
spl id: 6626e154-7292-4e59-a55e-93dbcc3f662b
spl set id: 732ed952-8b99-4756-874d-6211a651d005

Reported adverse events (FAERS/openFDA)#

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