Active Ingredient(s)

Isopropyl alcohol 75% v/v

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

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

500 mL NDC: 76687-005-13

500 mL NDC: 75239-006-13

V W
advance hand sanitizer spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:75239-006
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:75239-006-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
2	NDC:75239-006-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
3	NDC:75239-006-03	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
4	NDC:75239-006-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
5	NDC:75239-006-05	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
6	NDC:75239-006-06	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
7	NDC:75239-006-07	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
8	NDC:75239-006-08	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
9	NDC:75239-006-09	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
10	NDC:75239-006-10	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
11	NDC:75239-006-11	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
12	NDC:75239-006-12	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
13	NDC:75239-006-13	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
14	NDC:75239-006-14	650 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
15	NDC:75239-006-15	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
16	NDC:75239-006-16	3800 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
17	NDC:75239-006-17	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
18	NDC:75239-006-18	20000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
19	NDC:75239-006-19	50000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
20	NDC:75239-006-20	1000000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	05/15/2020

Labeler - Guangzhou Youxing Cosmetics CO.,LTD (544355953)

Name	Address	ID/FEI	Business Operations
Establishment
Guangzhou Youxing Cosmetics CO.,LTD.		544355953	manufacture(75239-006)

Youxing-Spray