BOLISI DISPSABLE HAND SANITIZER- alcohol solution

BOLISI Dispsable Hand Sanitizer by

Drug Labeling and Warnings

BOLISI Dispsable Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Guangzhou Baoli Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 75%±5% (V/V)

Purpose

 Antiseptic

Use

hand sanitizer to help decrease bacteria on the skin and recommended for repeated use.

KEEP OUT OF REACH OF CHILDREN

Children must be supervised in use of this product.

Warnings:

• For external use only.
• Flammable.
• Keep away from fire or flame.
• Do not apply around eyes.
• Do not use in ears and mouth.

When using this product, Avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if irritation or rash appears on the skin.

DOSAGE & ADMINISTRATION

Place enough product in your palm to thoroughly cover your hands rub together briskly until dry.

Children under 6 years of age should be supervised when using this product.

Other Information: 

• Do not store above 85℉.
• May discolor certain fabrics or surfaces.

Inactive ingredients

Water, Proplene Glycol, Triethanolamine, Carbomer.

Packaging

INGREDIENTS AND APPEARANCE

BOLISI DISPSABLE HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75255-002
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)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75255-002-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
2	NDC: 75255-002-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
3	NDC: 75255-002-03	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
4	NDC: 75255-002-04	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
5	NDC: 75255-002-05	100 mL in 1 TUBE; Type 0: Not a Combination Product	04/15/2020
6	NDC: 75255-002-06	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/14/2020

Labeler - Guangzhou Baoli Cosmetics Co., Ltd. (526940311)

Registrant - Guangzhou Baoli Cosmetics Co., Ltd. (526940311)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Baoli Cosmetics Co., Ltd.		526940311	manufacture(75255-002)