HAND SANITIZER- ethyl alcohol gel

hand sanitizer by

Drug Labeling and Warnings

hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Hangzhou Huiji Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

Use

■ Hand sanitizer to help decrease bacteria on
the skin
■When water, soap & towel are not
available.
■Recommended for repeated use,

WARNINGS

For external use only■Highly inflammable
Keep away from heat, sparks, open flame, hot surfaces.
Do not apply around eyes. Do not use in ears & mouth.
Avoid contact with eyes
If in eyes: rinse well with clean water
Stop use and seek medical advice or attention if
irritation persists

keep out of reach of children

Keep out of reach of children. Children must be
supervised in use of this product

Directions

■Squeeze the bottle after removing the lid and thoroughly
spread on both hands. Rub into skin until dry
Other Information Avoid contact with fabrics as
could cause discolouration

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73788-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER 934 (UNII: Z135WT9208)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73788-004-01	200 in 1 CARTON	05/29/2020
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 73788-004-02	150 in 1 CARTON	05/29/2020
2		60 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 73788-004-03	100 in 1 CARTON	05/29/2020
3		100 mL in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 73788-004-04	24 in 1 CARTON	05/29/2020
4		237 mL in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 73788-004-05	20 in 1 CARTON	05/29/2020
5		500 mL in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC: 73788-004-06	18 in 1 CARTON	05/29/2020
6		1000 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/29/2020

Labeler - Hangzhou Huiji Biotechnology Co., Ltd. (526893497)

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Huiji Biotechnology Co., Ltd.		526893497	manufacture(73788-004)