Ethyl Alcohol

Manufacturer
Progressive Products, LLC
Effective date
2023-03-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:54:31

Label at a glance#

ProductEthyl Alcohol
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizing wipes to help reduce bacteria on the skin.

Dosage and administration

Pull back canster lid Remove wipe Close canister lid Keep lid closed to retain moisture Wet hands thoroughly with product and allow to dry without wiping For single use only. Discard individual wipe after use

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizing wipes to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For External use only.

Flammable

SAFE HANDLING WARNING SECTION

Keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

  • in or near the eyes
  • on open skin wounds or burns

Stop use and ask a doctor

OTC - STOP USE SECTION

  • if irritation or redness develops
  • condition persists or get worse

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pull back canster lid
  • Remove wipe
  • Close canister lid
  • Keep lid closed to retain moisture
  • Wet hands thoroughly with product and allow to dry without wiping
  • For single use only. Discard individual wipe after use

Other information

OTHER SAFETY INFORMATION

  • Store at room temperature
  • Dispose of used wipe in trash, do not flush into toilet.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin, Fragrance, Benzalkonium chloride, Tocopherol Acetate, Citric Acid, Aloe Barbadensis Leaf Juice

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WAXIE

Hand Sanitizing Wipes

70% Alcohol Based

Kills 99.9% of germs

pic 2pic 2

pic 1pic 1

boxbox

12/240 CT CANISTERS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489307ethanol 70 % Medicated PadPSN1
1489307ethanol 0.7 ML/ML Medicated PadSCD1
1489307ethanol 70 % Medicated PadSY1
1489307ethanol 70 % Medicated WipesSY1
1489307ethyl alcohol 70 % ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67151-738-012025-01-30C16284748780-12cef2736-6790-d83d-e063-dadaa90ab31fHand Sanitizing Wipes 240ct

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67151-738-01Ethyl Alcohol1 mL in 1 PACKAGECLOTH11
67151-738-01Ethyl Alcohol240 in 1 BOXCLOTH2401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67151-738ETHYL ALCOHOL (HAND SANITIZING WIPES) CLOTH [PROGRESSIVE PRODUCTS, LLC]12 package rows20230318_f6c98ef2-91ba-f347-e053-6294a90abaf7.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67151-73867151-738-01

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
f6c98ef2-91bb-f347-e053-6294a90abaf7f6c98ef2-91ba-f347-e053-6294a90abaf72023-03-13WarningsExact identifier
spl id: f6c98ef2-91bb-f347-e053-6294a90abaf7
spl set id: f6c98ef2-91ba-f347-e053-6294a90abaf7

Reported adverse events (FAERS/openFDA)#

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