The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (70%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.

Sodium nitrite (0.09% v/v).

Sodium Benzoate (0.9% v/v).

Dimethylammonium (0.4% v/v)

Morpholine (o.1% v/v)

Triethylene Glycol (6.9% v/v)

Isobutane (28.00% v/v)

Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

in children less than 2 months of age
on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

sodium nitrate, sodium benzoate, dimethylammonium, morpholine, triethylene glycol, isobutane, purified water USP

Package Label - Principal Display Panel

200 mL NDC: 78358-001-02 200ml 125ml

500 ml NDC 78358-001-03 500ml

HAND SANITIZER
alcohol aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:78358-001
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
TRIETHYLENE GLYCOL (UNII: 3P5SU53360)	6 mL in 100 mL
SODIUM NITRITE (UNII: M0KG633D4F)	0.09 mL in 100 mL
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.09 mL in 100 mL
2,4,5-T DIMETHYLAMMONIUM (UNII: OQE98LYN9O)	0.4 mL in 100 mL
2,4-D MORPHOLINE (UNII: 62MSU01E50)	0.1 mL in 100 mL
ISOBUTANE (UNII: BXR49TP611)	28 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:78358-001-01	125 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/30/2020
2	NDC:78358-001-02	200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/30/2020
3	NDC:78358-001-03	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/30/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	03/30/2020

Labeler - Tecnología en Aerosol, S. de R.L. de C.V. (951578291)

Registrant - Tecnología en Aerosol, S. de R.L de C.V. (951578291)

Name	Address	ID/FEI	Business Operations
Establishment
Tecnología en Aerosol S. de R.L. de C.V.		951578291	manufacture(78358-001)