SANI-TOUCH HAND SANITIZER- ethyl alcohol gel

Sani-Touch by

Drug Labeling and Warnings

Sani-Touch 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.

Usage

Uses

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

Warnings

Warnings

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

Other Information

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

May discolor certain fabrics and surfaces.

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.

Inactive Ingredients

Acrylates/C 10/30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, FD&C Blue 1, FD&C Yellow 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E

Sani-Touch Front

Sani-Touch

Hand Sanitizer & Conditioner

TEC133

Dries Quickly. Hands Feel

Clean, Soothed and

Moisturized.

Kills 99.99%

15 Seconds

of Germs in

Fortified with Aloe Vera, Vitamin E                           Tomorrow’s Technology Today

18 fl. Oz                                                                                TECHNICIAN’S CHOICE®

                                                                                                PROFESSIONAL SERIES

5025-430-02 USF                                                                              Rev. 1.1

Sani_Touch Back

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/C 10/30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, FD&C Blue 1, FD&C Yellow 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E

Manufactured for                                            NOT TESTED ON ANIMALS

ECP, Incorporated

Woodridge, IL 60517

1-800-323-3521

www.technicianschoice.net

ECP and Technician’s Choice® are registered trademarks of ECP Incorporated © 2018

5025-430-02 USF                                              Rev. 1.1

Sani-Touch Case

                Sani-Touch

Hand Sanitizer & Conditioner

TEC133

Dries Quickly. Hands Feel

Clean, Soothed and

Moisturized.

Kills 99.99%

15 Seconds

of Germs in

Fortified with Aloe Vera, Vitamin E                           Tomorrow’s Technology Today

16/18 fl. Oz                                                                         TECHNICIAN’S CHOICE®

                                                                                                PROFESSIONAL SERIES

5025-430-02 USF                                                                              Rev. 1.0

INGREDIENTS AND APPEARANCE

SANI-TOUCH  HAND SANITIZER
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58575-181
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)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58575-181-01	800 mL in 1 POUCH; 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(58575-181)