U.S. LEGAL SUPPORT HAND SANITIZER- ethyl alcohol gel

U.S. Legal Support Hand Sanitizer by

Drug Labeling and Warnings

U.S. Legal Support 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

UsesI I 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 if redness or irritation
develop and persist for more than 72 hours.
Keep out of reach of children. Children must be
supervised in use of this product.

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

1 Do not store above 105°F
1 May discolor some fabrics

Inactive ingredients

Inactive Ingredients Water, Glycerin, Aloe
Barbadensis Leaf Extract, Carbomer,
Tocophery| Acetate, Triethanolamine.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

U.S. LEGAL SUPPORT HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73788-107
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
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER 934 (UNII: Z135WT9208)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73788-107-01	200 in 1 CARTON	08/12/2020
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 73788-107-02	150 in 1 CARTON	08/12/2020
2		60 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 73788-107-03	100 in 1 CARTON	08/12/2020
3		100 mL in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 73788-107-04	24 in 1 CARTON	08/12/2020
4		237 mL in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 73788-107-05	20 in 1 CARTON	08/12/2020
5		500 mL in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC: 73788-107-06	6 in 1 CARTON	08/12/2020
6		1000 mL in 1 BOTTLE; Type 0: Not a Combination Product
7	NDC: 73788-107-07	4 in 1 CARTON	08/12/2020
7		4000 mL in 1 BOTTLE; Type 0: Not a Combination Product
8	NDC: 73788-107-08	4 in 1 CARTON	08/12/2020
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	08/12/2020

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

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Huiji Biotechnology Co., Ltd.		526893497	manufacture(73788-107)