Alcohol Hand Wipe

Manufacturer
Eclectic Trade
Effective date
2020-06-04
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:16:04

Label at a glance#

ProductAlcohol Hand Wipe
Active ingredientBENZALKONIUM CHLORIDE, ALCOHOL
Label structure13 sections

Dosage and administration

Remove wipe Wet hands thoroughly with wipe and allow hands dry without wiping. Supervise children under 6 years of age when using this product to avoid swallowing. Remove wipe Wet hands thoroughly with wipe and allow hands dry without wiping. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store at room temprature May discolor certian fabrics or surfaces

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

The alcohol hand cleansing wipe is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (75%, volume/volume (v/v))
  2. Benzalkonium chloride(0.05% volume/volume (v/v))
  3. Water
  4. Menthol
  5. Glycerin

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. , Benzalkonium Chloride (0.05% v/v) Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Alcohol Hand Wipe

Use

INDICATIONS & USAGE SECTION

Alchohol Hand Wipe to help reduce bacteria on the skin when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

  • When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
  • Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
  • Do not apply large areas of skin

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Remove wipe
  • Wet hands thoroughly with wipe and allow hands dry without wiping.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

RECENT MAJOR CHANGES SECTION

  • Remove wipe
  • Wet hands thoroughly with wipe and allow hands dry without wiping.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store at room temprature
  • May discolor certian fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Menthol,Glycerin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

550gr NDC: 75501-005-12 120wipes120wipes

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75501-005-12Alcohol Hand Wipe550 g in 1 BAGCLOTH5504
75501-005-25Alcohol Hand Wipe150 g in 1 BAGCLOTH1504
75501-005-50Alcohol Hand Wipe225 g in 1 BAGCLOTH2254
75501-005-60Alcohol Hand Wipe270 g in 1 BAGCLOTH2704

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75501-005ALCOHOL HAND WIPE (ALCOHOL) CLOTH [ECLECTIC TRADE]4Legacy NDC, 4 package rows20200605_a561ac56-58d1-0d92-e053-2a95a90a9daa.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75501-00575501-005-12, 75501-005-25, 75501-005-60, 75501-005-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML · Source PDF

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
a7428da9-55aa-2d54-e053-2a95a90a99a0a561ac56-58d1-0d92-e053-2a95a90a9daa2020-06-04WarningsExact identifier
spl id: a7428da9-55aa-2d54-e053-2a95a90a99a0
spl set id: a561ac56-58d1-0d92-e053-2a95a90a9daa

Reported adverse events (FAERS/openFDA)#

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