HAND SANITIZER- alcohol spray

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Saje Natural Business Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 68% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Product Identity

Hand Sanitizer - Antibacterial Spray

2 fl oz | 60 ml

3.4 fl oz | 100 ml
6.8 fl oz | 200 ml
33.8 fl oz | 1 L

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

When using this product keep out of eyes, ears, and mouth. If contact occurs with eyes, rinse 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, contact a Poison Control Center right away or get medical help right away.

STOP USE

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

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

Directions

• Spray 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

aloe barbadensis leaf juice powder, glycerin, lime oil, purified water.

Hand Sanitizer Spray - Package Label

60 mL NDC: 70983-025-04

100 mL NDC: 70983-025-01

200 mL NDC: 70983-025-02

1 L NDC: 70983-025-03

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70983-025
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	68 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LIME OIL (UNII: UZH29XGA8G)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70983-025-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
2	NDC: 70983-025-02	200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
3	NDC: 70983-025-03	1000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/26/2020
4	NDC: 70983-025-04	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/02/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/01/2020

Labeler - Saje Natural Business Inc. (080465432)