AccuBan Gel

Manufacturer
TEL Group LLC
Effective date
2020-10-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:05

Label at a glance#

ProductAccuBan Gel
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thoroughly for at lest 15 seconds Allow to air dry Supervise use by children

Storage and handling

Store below 105F (41C) May be damaging or discoloring to certain fabrics, wood, plastics and decorative finishes.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v ........ antimicrobial

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Avoid contact with open flames.

OTC - WHEN USING SECTION

Avoid contact with eyes.  If contact occurs flush immediately with plenty of water.

External use only

OTC - STOP USE SECTION

Stop use immediately if redness or irritation occurs and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, seek medical attention right away or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly for at lest 15 seconds
  • Allow to air dry
  • Supervise use by children

Other information

STORAGE AND HANDLING SECTION

Store below 105F (41C)

May be damaging or discoloring to certain fabrics, wood, plastics and decorative finishes.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, PEG-6 (and) AMP Acrylates/Vinyl Isodecanoate Crosspolymer, Isononyl Isononanoate, Isopropyl Myristate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80620-110-012022-01-28C16284748780-1d6a99b39-6389-a426-e053-dadaa90af4c29a07f276-9dc2-4dde-a881-a359554554f1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80620-110-01AccuBan Gel.237 L in 1 BOTTLE, PLASTICSOLUTION.2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80620-110ACCUBAN GEL (ALCOHOL) SOLUTION [TEL GROUP LLC]1Legacy NDC, 1 package rows20201021_9a07f276-9dc2-4dde-a881-a359554554f1.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80620-11080620-110-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT

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
5b44eee8-191e-4b5b-9739-7dd02ccf592a9a07f276-9dc2-4dde-a881-a359554554f12020-10-19WarningsExact identifier
spl id: 5b44eee8-191e-4b5b-9739-7dd02ccf592a
spl set id: 9a07f276-9dc2-4dde-a881-a359554554f1

Reported adverse events (FAERS/openFDA)#

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