HAND SANITIZER- hand sanitizer spray spray

Hand sanitizer by

Drug Labeling and Warnings

Hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Guangzhou Baihua Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Use

Hand sanitizer to decrease bacteria on the skin, Recommended for repeated use.

Warnings

For external use only
Flammable, keep away from fire or flame

Do not use

if irritation and rash occurs. These may be signs of serious condition.

When Using

When using this product keep out of eye, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Avoid contact with broken skin

Stop Use

Stop use and ask a doctor if irritation and rash occurs. These may be signs of serious condition.

Ask Doctor

Stop use and ask a doctor if irritation and rash occurs. These may be signs of serious condition.

Keep Out Of Reach Of Children

Keep out of reach of children, if swallowed, get medical help or contact a poison control center right away

Directions

Spray enough product in your palm to thoroughly cover your hands, rub hands together briskly until dry, recommended to repeated use, children under 6 years of age should be supervised when using this product

Other information

Protect the product in this container from excessive heat and direct sun.
Store below 104 °F(40 °C)
May discolorcertain fabrics

Inactive ingredients

Water, Fragrance, Aloe Barbadensis Leaf Water,Glycerin, Tocopheryl Acetate, Yellow 6 (Cl 15985), Red 33(C1 17200)

Questions

Call 718-975-2586

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
hand sanitizer spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77665-105
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
RED 33 (UNII: 9DBA0SBB0L)
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
FRAGRANCE 13576 (UNII: 5EM498GW35)
YELLOW 6 (UNII: H77VEI93A8)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77665-105-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/24/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/24/2025

Labeler - Guangzhou Baihua Co., Ltd (545015588)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Baihua Co., Ltd		545015588	manufacture(77665-105)