FDA.reportPublic FDA data

Antimicrobial Alcohol Gel Hand wipe

Manufacturer
Geri-Gentle Corporation
Effective date
2023-11-10
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:21:12

Label at a glance#

ProductAntimicrobial Alcohol Hand
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Antiseptic  For handwashing to decrease bacteria on the skin, assisting ill persons, and before contact with a person under medical care or treatment Apply topically to the skin to help prevent cross-contamination Recommended for repeated use  Dries in seconds

Dosage and administration

To start feed: Remove cover and discard seal from container. From center of toweled roll, pull up wipe corner, tear off fist wipe for use. Twist next wipe into a point and thread through the hole in the container cover. Pull through about one inch. Replace cover. Pull out wipes as needed and snap off at 90° angle. Keep cap closed to prevent moisture loss Wipe hands , fingers, interdigital areas and wrists thorough...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 65.9% by volume

Purpose

OTC - PURPOSE SECTION

Antiseptic  

Uses

INDICATIONS & USAGE SECTION

  • Antiseptic 
  • For handwashing to decrease bacteria on the skin, assisting ill persons, and before contact with a person under medical care or treatment
  • Apply topically to the skin to help prevent cross-contamination
  • Recommended for repeated use 
  • Dries in seconds

Warnings

WARNINGS SECTION

  • Flammable, keep away from fire or flame
  • For external use only

Do not use

OTC - DO NOT USE SECTION

  • in or make contact with the eyes
  • Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a physician 

Keep this our 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 Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

  • To start feed: Remove cover and discard seal from container. From center of toweled roll, pull up wipe corner, tear off fist wipe for use. Twist next wipe into a point and thread through the hole in the container cover. Pull through about one inch. Replace cover. Pull out wipes as needed and snap off at 90° angle. Keep cap closed to prevent moisture loss
  • Wipe hands , fingers, interdigital areas and wrists thoroughly with towelette. Be sure to utilize the entire wipe surface. Allow to dry
  • If hands are visibly soiled or contaminated, use first wipe to clean hands, then discard wipe, Sanitize with a second wipe
  • Discard after single use

Other information

SPL UNCLASSIFIED SECTION

Lot No. and Expiration Date can be found on canister

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Tetrasodium EDTA

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 2Label 2

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
69771-00269771-002-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
EDETATE SODIUMMP1J8420LUIACT
ALCOHOL3K9958V90MACTIB

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
2a9fb101-ae95-0f6a-e063-6294a90a5dfeccde8b53-207a-42ee-a8c3-ebbae2c8a1cd2025-01-01WarningsExact identifier
spl set id: ccde8b53-207a-42ee-a8c3-ebbae2c8a1cd

Reported adverse events (FAERS/openFDA)#

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