BORTEK HAND SANITIZER- ethyl alcohol gel

bortek by

Drug Labeling and Warnings

bortek by is a Otc medication manufactured, distributed, or labeled by Inopak, Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Keep out of reach of children

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

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

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

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

Administration

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

Bortek Hand Sanitizer Front

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 Hand Sanitizer Back Lable

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 Hand Sanitizer Case label

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

EQUIPMENTPARTSRENTALSSERVICESUPPLIES

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

INGREDIENTS AND APPEARANCE

BORTEK  HAND SANITIZER
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58575-180
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
aloe (UNII: V5VD430YW9)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58575-180-01	540 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/02/2020
2	NDC: 58575-180-02	8640 mL in 1 CASE; Type 0: Not a Combination Product	01/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/02/2020

Labeler - Inopak, Ltd (194718243)

Establishment
Name	Address	ID/FEI	Business Operations
Inopak, Ltd		194718243	manufacture(58575-180)