FDA.reportPublic FDA data

Bortek® Gel Hand Sanitizer 180

Manufacturer
Inopak, Ltd
Effective date
2020-02-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:41:55

Label at a glance#

Productbortek Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

To decrease bacteria on the skin that potentially can cause disease. Recommended for repeated use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Children should be supervised by an adult when using this product.

Ask Doctor

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation and redness develop or if condition persists for more than 72 hours.

Uses

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin that potentially can cause disease.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

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

Keep out of eyes, ears, or mouth. In case of eye contact, flush eyes with water

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop or if condition persists for more than 72 hours.

Administration

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply sufficient amount of product to your palm to cover both hands.
  • Rub until dry.

Other Information

OTHER SAFETY INFORMATION

May discolor certain fabrics and surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10/30, Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, FD&C Blue No. 1, FD&C Yellow No. 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E, Water

Bortek Hand Sanitizer Front

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BORTEK INDUSTRIES, INC.

Gel Hand Sanitizer

WITH ALOE VERA, VITAMIN E,

& MOISTURIZERS

ILLS 99.99% OF GERMS

18 FL OZ

PART # 5025-Bortek

Rev. 1.0

Bortek Front LabelBortek Front Label

Bortek Hand Sanitizer Back Lable

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Part # 5025-Bortek

Rev 1.0

DRIES QUICKLY, LEAVES SKIN

FEELING SOOTHED AND MOISTURIZED

Drug Facts

Drug Facts

Active Ingredient                                             Purpose

Ethyl Alcohol 70% v/v……………………………Antiseptic

Uses

  • To decrease bacteria on the skin that potentially can cause disease.
  • Recommended for repeated use.

Warnings

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

Keep out of eyes, ears, or mouth. In case of eye contact, flush eyes with water

Stop use and ask a doctor if irritation and redness develop or if condition persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Children should be supervised by an adult when using this product.

Directions

  • Apply sufficient amount of product to your palm to cover both hands.
  • Rub until dry.

Other Information

May discolor certain fabrics and surfaces.

Inactive ingredients

Acrylates/C10/30, Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, FD&C Blue No. 1, FD&C Yellow No. 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E, Water

A FAMILY COMPANY 1967

Reorder Item #:                      Bortek®                                             800.626.7835

2813011                                INDUSTRIES, INC.                             sweeperland.com

Bortek BackBortek Back

Bortek Hand Sanitizer Case label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rev 1.0                                  A FAMILY COMPANY SINCE 1967

Part#: 5025-BortekCS

Bortek®

INDUSTRIES, INC.

GEL HAND SANITIZER

                                MADE IN THE USA

YOUR CLEANING SOLUTIONS RESOURCE®

                800.626.7835

                Sweeperland.com

Corporate Headquarters

4713 Gettysburg Road

Mechanicsburg, PA 17055

EQUIPMENT•PARTS•RENTALS•SERVICE•SUPPLIES

Ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadenis Leaf Juice, FD&C Blue No. 1, FD&C Yellow No. 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E, Water

Reorder Item #: 28130111             Net Contents: 16 X 18 FL OZ

Bortek CaseBortek Case

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
58575-18058575-180-01, 58575-180-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
aloeV5VD430YW9IACT
ALCOHOL3K9958V90MACTIB
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
ISOPROPYL ALCOHOLND2M416302IACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
WATER059QF0KO0RIACT

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
bfcceb3d-4aeb-5e3e-e053-2a95a90a46e1bf35d3ca-9f08-45ba-9abd-05d033cb27ee2021-04-12WarningsExact identifier
spl set id: bf35d3ca-9f08-45ba-9abd-05d033cb27ee

Reported adverse events (FAERS/openFDA)#

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