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, and 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, Fragrance

Package Label - Principal Display Panel

30 mL NDC: 75601-1271-1 30 mL NDC: 75601-1271-2

INGREDIENTS AND APPEARANCE

CLEANSLATE 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75601-1004
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)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75601-1004-2	1 in 1 BOX	10/14/2020
1	NDC: 75601-1004-1	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(75601-1004)

Establishment
Name	Address	ID/FEI	Business Operations
Punch Studio, LLC		843912440	relabel(75601-1004)