Active Ingredient(s)

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

Disinfectant Spray

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

water

Package Label - Principal Display Panel

500ml label spray 500 mL NDC: 76714-002-01

200 mL NDC: 76714-002-02 200ml spray

500 mL NDC:76714-002-03 500 AURA

300 mL NDC:76714-002-04 300 AURA

360mL NDC: 76714-002-05 360 AURA

DISINFECTANT
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76714-002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	375 mL in 500 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)	125 mL in 500 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:76714-002-01	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/30/2020
2	NDC:76714-002-02	200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/30/2020
3	NDC:76714-002-03	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/30/2020
4	NDC:76714-002-04	300 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/30/2020
5	NDC:76714-002-05	360 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/30/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	04/30/2020

Labeler - Guangdong Yawei Bioscience Co., Ltd (543334955)

Name	Address	ID/FEI	Business Operations
Establishment
Guangdong Yawei Bioscience Co., Ltd		543334955	manufacture(76714-002)