ANTIBACTERIAL HAND SANITIZER- ethyl alcohol gel

Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Twintech Industry, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Use

• decreases bacteria and germs on the hands
• when water, soap & towel are not available
• recommended for repeated use

Warnings

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

Stop use and ask a doctor if

irritation or redness develops or persists.

Do not apply around eyes.

Do not use

in ears & mouth

When using this product,

avoid contact with eyes. In case of contact flush eyes with water.

Keep out of reach of children.

Children under 6, use only under adult supervision. Not recommended for infants.

Directions

• pump as needed into your palms and thoroughly spread on both hands
• rub into skin until dry

Other information

• store at 20 ℃ (68 ℃ to 77 ℉).
• may discolor fabrics

Inactive Ingredients

Purified water, triethanolamine, glycerine, Disodium EDTA, carbomer

Package/Label Principal Display Panel

Antibacterial Hand Sanitizer
1.8 fl. oz. (54ML)

Distributed by:
TWINTECH INDUSTRY, INC.
Cerritos, CA          Made in China

Label

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76700-309
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76700-309-01	54 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/02/2020
2	NDC: 76700-309-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/02/2020
3	NDC: 76700-309-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/02/2020
4	NDC: 76700-309-04	238 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/02/2020
5	NDC: 76700-309-05	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/02/2020

Labeler - Twintech Industry, Inc. (136388423)