GERMisept Antibacterial Hand Sanitizing Alcohol Wipes

Manufacturer
Innovent Inc
Effective date
2023-12-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:05:25

Label at a glance#

ProductGERMisept Antibacterial Hand Sanitizing Alcohol Wipes
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

For cleansing to decrease bacteria on skin. Recommended for repeated use with a new unused wipe each time. Dries quickly.

Dosage and administration

Open the top cover, and tear the top sealing Pick wipe from center of roll, and thread wipe through the center of lid. Pull wipes to use. Wipe hands thoroughly with product and allow to dry without wiping. Close lid after use to retain moisture.

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 cleansing to decrease bacteria on skin.
  • Recommended for repeated use with a new unused wipe each time.
  • Dries quickly.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

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

Keep this 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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Open the top cover, and tear the top sealing
  • Pick wipe from center of roll, and thread wipe through the center of lid. Pull wipes to use.
  • Wipe hands thoroughly with product and allow to dry without wiping.
  • Close lid after use to retain moisture.

Other information

SPL UNCLASSIFIED SECTION

  • Dispose of wipe in the proper container.
  • Do not flush down the toilet.

*Kill Claims Against: E.Coli & Staphylococcus

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Aqua (Purified & De-Ionized Water), Benzalkonium Chloride, Glycerin.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bag2Bag2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN3
1307051ethanol 0.75 ML/ML Medicated PadSCD3
1307051ethanol 75 % Hand Sanitizer WipesSY3
1307051ethyl alcohol 75 % Topical ClothSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70335-011-01GERMisept Antibacterial Hand Sanitizing Alcohol Wipes50 in 1 PACKAGECLOTH503
70335-011-01GERMisept Antibacterial Hand Sanitizing Alcohol Wipes4 in 1 BAGCLOTH43

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70335-011GERMISEPT ANTIBACTERIAL HAND SANITIZING ALCOHOL WIPES (ALCOHOL) CLOTH [INNOVENT INC]3Current NDC, Legacy NDC, 2 package rows20231222_ba49c5cd-295a-dd32-e053-2a95a90aec03.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70335-01170335-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
GERMisept Antibacterial Hand Sanitizing Alcohol WipesALCOHOLInnovent Incba49c5cd-295a-dd32-e053-2a95a90aec032023-12-21WarningsExact identifier
ndc (package): 70335-011-01
ndc (product): 70335-011
ndc11 (package): 70335001101
spl id: 0d0d6d39-a9c7-e084-e063-6394a90af89e
spl set id: ba49c5cd-295a-dd32-e053-2a95a90aec03

Reported adverse events (FAERS/openFDA)#

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