SANAUX HAND SANITIZER ANTIBACTERIAL GEL- alcohol gel

Sanaux Hand Sanitizer Antibacterial Gel by

Drug Labeling and Warnings

Sanaux Hand Sanitizer Antibacterial Gel by is a Otc medication manufactured, distributed, or labeled by SANLOZ GROUP INC., SANLOZ MATERIALES AVANZADOS S.A.P.I. DE C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70% v/v.

Purpose

Antibacterial   

Uses

Hand sanitizer to help reduce bacteria on skin.

Warnings

Keep out of reach of children.

When using this product, do not use in or near the eyes. In case of exposure in eyes wash thoroughly with lots of water.

If swallowed do not attempt to induce vomit, seek medical attention or contact poison control center immediately.

This product is intended for external use only. Flammable. Keep away from fire or flame.

Directions

Place enough product in your palm to thoroughly cover both hands. Rub hand together briskly until dry. Children under 6 years of age should be supervised when using this product.

KEEP OUT OF REACH OF CHILDREN

Inactive ingredients

Glycerin, Carboxymethylcellulose, Triethanolamine, Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SANAUX HAND SANITIZER ANTIBACTERIAL GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75509-001
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
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75509-001-01	30 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
2	NDC: 75509-001-02	50 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
3	NDC: 75509-001-03	60 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
4	NDC: 75509-001-04	100 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
5	NDC: 75509-001-05	200 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
6	NDC: 75509-001-06	240 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
7	NDC: 75509-001-07	250 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
8	NDC: 75509-001-08	500 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
9	NDC: 75509-001-09	900 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
10	NDC: 75509-001-10	1000 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
11	NDC: 75509-001-11	1890 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
12	NDC: 75509-001-12	3780 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
13	NDC: 75509-001-13	18900 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
14	NDC: 75509-001-14	200000 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
15	NDC: 75509-001-15	1000000 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/15/2020

Labeler - SANLOZ GROUP INC. (114596838)

Establishment
Name	Address	ID/FEI	Business Operations
SANLOZ MATERIALES AVANZADOS S.A.P.I. DE C.V.		951576561	manufacture(75509-001)