ADVANCED HAND SANITIZER- alcohol gel

Advanced Hand Sanitizer by

Drug Labeling and Warnings

Advanced Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by UNISOURCES GROUP LLC, Hangzhou Huiji Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl alcohol 72%

Purpose

Antiseptic

Uses

• Hand sanitizer to help reduce bacteria on the skin
• Recommended for repeated use

Warnings

• Flammable, Keep away from fire or flame.
• For external use only.

Do not use 

• in or near the eyes. in case of contact, flush eyes with water.

Stop use and ask a doctor if

• irritation or rash appears and lasts.

Keep out of reach of children.

• If need, get medical help or contact a Poison Control Center.

Directions

• Wet hands thoroughly with enough product and allow to dry without wiping.
• Children under 6 years of age use only under adult supervision when using this product.

Other information

• Store below 105°F(43 C)
• Surface to wood and plastics.
• May discolor certain fabrics or surfaces

Inactive ingredients

Water, Glycerin, Aloe barbadensis leaf extract, Carbomer, Tocopheryl Acetate, Triethanolamine.

Package Labeling: 59mL

Package Labeling: 236mL

Package Labeling: 295mL

INGREDIENTS AND APPEARANCE

ADVANCED HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75311-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.72 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75311-000-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/31/2020
2	NDC: 75311-000-02	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/31/2020
3	NDC: 75311-000-03	295 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/31/2020

Labeler - UNISOURCES GROUP LLC (117474227)

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Huiji Biotechnology Co., Ltd.		526893497	manufacture(75311-000)