FDA.reportPublic FDA data

Ethyl alcohol wet wipes

Manufacturer
ProStock LLC
Effective date
2020-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:40

Label at a glance#

ProductEthyl alcohol wet wipes
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For hand-washing to decrease bacteria on skin

Dosage and administration

Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation.  Thoroughly wipe hands, allow to dry without washing. Discard after single use

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol (70.00% V/V)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand-washing to decrease bacteria on skin

Warnings

WARNINGS SECTION

Flammable. Keep away from heat and flame.
For External use only.

Do not use

OTC - DO NOT USE SECTION

in eyes. In case of contact, rinse thoroughly with water.

Stop use & ask doctor

OTC - STOP USE SECTION

if rash/redness or irritation appears/develops and persist for more than 72 hours.

Keep out of reach from children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

Directions

DOSAGE & ADMINISTRATION SECTION

  • Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation. 
  • Thoroughly wipe hands, allow to dry without washing.
  • Discard after single use

Other information

SPL UNCLASSIFIED SECTION

  • Do not flush down toilet. 
  • Keep away from sunlight. Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit) 
  • May discolor certain fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Aloe Barbadensis Leaf Juice, D-Panthenol, Phenoxyethanol

Package Labeling:15pcs

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:50pcs

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

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
73796-003-022023-01-30C16284748780-1f386c649-b75d-0266-e053-dadaa90a7c1aEthyl alcohol wet wipes
73796-003-032023-01-30C16284748780-1f386c649-b75d-0266-e053-dadaa90a7c1aEthyl alcohol wet wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73796-003-02Ethyl alcohol wet wipes15 in 1 PACKAGECLOTH151
73796-003-02Ethyl alcohol wet wipes3.6 mL in 1 PATCHCLOTH3.61
73796-003-03Ethyl alcohol wet wipes3.6 mL in 1 PATCHCLOTH3.61
73796-003-03Ethyl alcohol wet wipes50 in 1 PACKAGECLOTH501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73796-003ETHYL ALCOHOL WET WIPES (ALCOHOL) CLOTH [PROSTOCK LLC]1Legacy NDC, 4 package rows20200918_af850c7d-da64-7a4e-e053-2a95a90a6683.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
73796-00373796-003-02, 73796-003-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
DEXPANTHENOL1O6C93RI7ZIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALCOHOL3K9958V90MACTIB

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
af850b5e-c99e-3d4e-e053-2995a90a7948af850c7d-da64-7a4e-e053-2a95a90a66832020-09-17WarningsExact identifier
spl id: af850b5e-c99e-3d4e-e053-2995a90a7948
spl set id: af850c7d-da64-7a4e-e053-2a95a90a6683

Reported adverse events (FAERS/openFDA)#

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