Active Ingredient(s)

Alcohol 72% v/v.

Purpose

Antiseptic

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, glycerin, Arcylates/vinyl, isodecanote cross polymer, amino ethyl propanol, Panthenol, Aloe Barbados leaf juice, Tocopheryl Acetate

Package Label - Principal Display Panel

label

ADVANCED HAND SANITIZER
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:75144-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
ISODECYL ALCOHOL (UNII: 3160X491M7)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM ACRYLATE (UNII: 7C98FKB43H)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:75144-001-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC:75144-001-02	69 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC:75144-001-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC:75144-001-04	125 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
5	NDC:75144-001-05	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/30/2020
6	NDC:75144-001-06	308 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/30/2020
7	NDC:75144-001-07	502 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/30/2020
8	NDC:75144-001-08	1000 mL in 1 BOTTLE, PUMP; 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 - Bellapierre Cosmetics Inc (802861802)

Name	Address	ID/FEI	Business Operations
Establishment
ZheJiang Ushas Cosmetics Co., Ltd		544910474	manufacture(75144-001)

Advanced Hand Sanitizer