Alcohol Wet Wipes

Manufacturer
Robert Gordon Ind. Ltd.
Effective date
2023-03-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:54:37

Label at a glance#

ProductAlcohol Wet Wipes
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin

Dosage and administration

Tear open packet and remove wipe. Wet hands thoroughly with product and let hands air dry. Throw used wipe in trash. Do not flush.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% (v/v)

purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the 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

When Using this product

OTC - STOP USE SECTION

  • avoid contact with eyes and mouth. If in ayes, flush thoroughly with water.
  • Discontinue use and contact a doctor if irritation and redness develop and conditions persis for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Tear open packet and remove wipe.
  • Wet hands thoroughly with product and let hands air dry.
  • Throw used wipe in trash. Do not flush.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Water

Major changes

RECENT MAJOR CHANGES SECTION

Uses - to decrease bacteria on the skin

Dosage and administration - Apply to clean and sterilizc hands, household and office objects,cellphone, computers,desks etc, and discard.

Other Information

OTHER SAFETY INFORMATION

  • Store between 15-30 oC (59-86 oF)
  • Avoid freezing and excessive heat above 40 oC (104 oF)

Package Labeling:10count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol 10x labelAlcohol 10x label

Package Labeling:40count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle6Bottle6

Package Labeling:80count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle7Bottle7

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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74979-006-01Alcohol Wet Wipes10 in 1 PACKAGECLOTH102
74979-006-01Alcohol Wet Wipes4.5 mL in 1 PATCHCLOTH4.52
74979-006-02Alcohol Wet Wipes4.75 mL in 1 PATCHCLOTH4.752
74979-006-02Alcohol Wet Wipes40 in 1 PACKAGECLOTH402
74979-006-03Alcohol Wet Wipes80 in 1 PACKAGECLOTH802
74979-006-03Alcohol Wet Wipes4.75 mL in 1 PATCHCLOTH4.752

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74979-006ALCOHOL WET WIPES (ALCOHOL) CLOTH [ROBERT GORDON IND. LTD.]2Legacy NDC, 6 package rows20230331_b062682a-bae4-5cc7-e053-2a95a90a2694.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74979-00674979-006-01, 74979-006-02, 74979-006-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
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
f7e66dcd-8f27-b52c-e053-6294a90a0433b062682a-bae4-5cc7-e053-2a95a90a26942023-03-27WarningsExact identifier
spl id: f7e66dcd-8f27-b52c-e053-6294a90a0433
spl set id: b062682a-bae4-5cc7-e053-2a95a90a2694

Reported adverse events (FAERS/openFDA)#

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