CLEANSLATE- alcohol liquid

Cleanslate by

Drug Labeling and Warnings

Cleanslate by is a Otc medication manufactured, distributed, or labeled by Punch Studio, LLC, Ningbo Pretty Tourism Manufacture Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75% Purpose: Antiseptic

Purpose

Antiseptic

Use

To help reduce bacteria on hands when water & soap are not available

Warnings

For external use only

Flammable, keep away from heat or flame

Do not use

Do not use

• On children less than 2 years old
• On open skin wounds

When using this product

When using this product keep out of eyes, ears & mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if

Stop use and ask a doctor if skin irritation occurs.

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

• Apply onto hands thoroughly, rub together until dry
• Supervise children under 6 years old

Other information

• Store between 15-30°C (59-86°F)
• Avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

Water, Aminomethyl Propanol, Carbomer, Glycerin, Propylene Glycol, Aloe Barbadensis Extract, Tocopheryl Acetate

Package Label - Principal Display Panel

30 mL NDC: 75601-1270-1 30 mL NDC: 75601-1270-2

INGREDIENTS AND APPEARANCE

CLEANSLATE 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75601-1003
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
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75601-1003-2	1 in 1 BOX	10/14/2020
1	NDC: 75601-1003-1	30 mL in 1 BOTTLE, SPRAY; 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	part333A	10/14/2020

Labeler - Punch Studio, LLC (843912440)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Pretty Tourism Manufacture Co., Ltd.		553193489	manufacture(75601-1003)

Establishment
Name	Address	ID/FEI	Business Operations
Punch Studio, LLC		843912440	relabel(75601-1003)