PL Hand Sanitizer Wipe

Manufacturer
Newport MFG LLC
Effective date
2020-10-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:32:12

Label at a glance#

ProductPL Hand Sanitizer Wipe
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thouroughly with product and allow to dry without wiping. for children under 5, use only with adult supervision. not recommended for use on infants

Storage and handling

Store between 20-25C (67-77F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

  • To decrease bacteria on skin
  • Recommended for repeated use

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.

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

  • Wet hands thouroughly with product and allow to dry without wiping.
  • for children under 5, use only with adult supervision.
  • not recommended for use on infants

Other information

STORAGE AND HANDLING SECTION

  • Store between 20-25C (67-77F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Citrus Limon Peel Oil, D-Limonene, Glycerin, Tocopherol Acetate (Vitamin E), Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3 mL NDC: 80479-275-69

NDC 80479-275-69NDC 80479-275-69

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN2
1307051ethanol 0.75 ML/ML Medicated PadSCD2
1307051ethanol 75 % Hand Sanitizer WipesSY2
1307051ethyl alcohol 75 % Topical ClothSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80479-275-692022-01-28C16284748780-1d6a99b39-e513-a426-e053-dadaa90af4c2PL Hand Sanitizer Wipe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80479-275-69PL Hand Sanitizer Wipe3 mL in 1 POUCHCLOTH32

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80479-275PL HAND SANITIZER WIPE (ALCOHOL) CLOTH [NEWPORT MFG LLC]2Legacy NDC, 1 package rows20201022_b140d93a-f5ff-7552-e053-2995a90ac633.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80479-27580479-275-69

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
b236b420-3583-355d-e053-2995a90a9a3fb140d93a-f5ff-7552-e053-2995a90ac6332020-10-21WarningsExact identifier
spl id: b236b420-3583-355d-e053-2995a90a9a3f
spl set id: b140d93a-f5ff-7552-e053-2995a90ac633

Reported adverse events (FAERS/openFDA)#

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