PAU DISPOSABLE HAND SANITIZER- alcohol solution

PAU Disposable Hand Sanitizer by

Drug Labeling and Warnings

PAU Disposable 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 65%±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, Aminomethyul Propanol, Carbomer.

Packaging

INGREDIENTS AND APPEARANCE

PAU DISPOSABLE HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75255-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER 934 (UNII: Z135WT9208)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75255-004-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
2	NDC: 75255-004-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
3	NDC: 75255-004-03	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
4	NDC: 75255-004-04	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/14/2020

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(75255-004)