MEDI-WIPES

Manufacturer
Western First Aid Safety dba Aramark | Lights Medical Manufacture Co., Ltd.
Effective date
2021-05-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:40:28

Label at a glance#

ProductMEDI-WIPES
Active ingredientALCOHOL, CHLOROXYLENOL
Label structure10 sections

Indications and uses

For hand washing to decrease bacteria on skin when soap and water are not available.

Dosage and administration

tear packet open, remove towelette wipe hands/wrist areas for 15 seconds and discard

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Ethyl Alcohol 40.0%

Chloroxylenol (PCMX) 0.5%

Purpose

OTC - PURPOSE SECTION

Ethyl Alcohol ................ Antiseptic

Chloroxylenol (PCMX) .... Antiseptic

Uses:

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on skin when soap and water are not available.

Warnings:

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame

When Using The Product:

OTC - WHEN USING SECTION

  • do not get into eyes, if contact occurs rinse eye thoroughly with water

Stop Use And Ask Doctor If:

OTC - STOP USE SECTION

  • if irritation or redness develop and persist for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of Reach Of Children:

If swallowed, get medical help or contact a Poison Control center right away. 1-800-222-1222

Directions:

DOSAGE & ADMINISTRATION SECTION

  • tear packet open, remove towelette
  • wipe hands/wrist areas for 15 seconds and discard

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

aloe vera, fragrance, purified water

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MEDI-WIPES

AntimicrobialTowelette

With PCMX and ALOE

• Non-Drying
• Meets OSHA Requirements
• Decreases Bacteria On Skin
• Use For Hand Washing
  When Soap And Water
  Are Not Available

               NDC# 81238-5104-1

aramarkThe First Choice In First Aid

Manufactured for Aramark   Lenexa, KS 66219  913-269-9611

LOT

Medi-wipesMedi-wipes

res

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1483212chloroxylenol 0.5 % / ethanol 40 % Medicated PadPSN2
1483212chloroxylenol 5 MG/ML / ethanol 0.4 ML/ML Medicated PadSCD2
1483212chloroxylenol 0.5 % / ethanol 40 % Medicated WipeSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81238-5104-12023-01-30C16284748780-1f386c64a-43b2-0266-e053-dadaa90a7c1aaramark MEDI-WIPES Antimicrobial Towelette

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81238-5104-1MEDI-WIPES1.5 g in 1 PACKETCLOTH1.52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81238-5104MEDI-WIPES (ETHYL ALCOHOL, CHLOROXYLENOL) CLOTH [WESTERN FIRST AID SAFETY DBA ARAMARK]2Legacy NDC, 1 package rows20210522_74324fbf-e96e-46aa-a563-c6b1d80ca00c.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81238-510481238-5104-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
aa59a5c8-385e-4a05-85d5-dbdf06cea55d74324fbf-e96e-46aa-a563-c6b1d80ca00c2021-05-21WarningsExact identifier
spl id: aa59a5c8-385e-4a05-85d5-dbdf06cea55d
spl set id: 74324fbf-e96e-46aa-a563-c6b1d80ca00c

Reported adverse events (FAERS/openFDA)#

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