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 70%

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■ Flammable
Keep away from fire or flame
Do not apply around eyes. Do not use in ears & mouth.
When using this product. avoid contact with eyes.
In case of contact flush eyes with water
Stop use and ask a doctor it redness or irritation
develop and persist for more than 72 hours

keep out of reach of children

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

Directions

Pump as needed into your palms and thoroughly
spread on both hands. Rub into skin until dry
Other Information Store at 20C(88" to 77"F)
may discolor fabrices

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: 73788-002
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: 73788-002-01	200 in 1 CARTON	03/21/2020
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 73788-002-02	150 in 1 CARTON	03/21/2020
2		60 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 73788-002-03	100 in 1 CARTON	03/21/2020
3		100 mL in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 73788-002-04	24 in 1 CARTON	03/21/2020
4		237 mL in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 73788-002-05	20 in 1 CARTON	03/21/2020
5		500 mL in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC: 73788-002-06	18 in 1 CARTON	03/21/2020
6		1000 mL in 1 BOTTLE; Type 0: Not a Combination Product
7	NDC: 73788-002-07	4 in 1 CARTON	03/21/2020
7		3780 mL in 1 BOTTLE; Type 0: Not a Combination Product
8	NDC: 73788-002-08	4 in 1 CARTON	03/21/2020
8		5000 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	03/21/2020

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

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Huiji Biotechnology Co., Ltd.		526893497	manufacture(73788-002)