Hand Sanitizer

Manufacturer: Punch Studio, LLC | Ningbo Pretty Tourism Manufacture Co., Ltd.
Effective date: 2022-01-12
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-05-31 23:46:38

Label at a glance#

ProductCleanslate

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

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

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

Do not use

On children less than 2 years old
On open skin wounds

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation occurs.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 mL NDC: 75601-1271-1 Front & back labels30 mL NDC: 75601-1271-2 Outer box

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1047755	ethanol 75 % Topical Solution	PSN	5
1047755	ethanol 0.75 ML/ML Topical Solution	SCD	5
1047755	ethanol 75 % Topical Solution	SY	5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75601-1004-2	2023-07-28	C162847	48780-1	0191ceaa-704f-198a-e063-dbdaa90aec3e	Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75601-1004-1	Cleanslate	30 mL in 1 BOTTLE, SPRAY	LIQUID	30		5
75601-1004-2	Cleanslate	1 in 1 BOX	LIQUID	1		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75601-1004	CLEANSLATE (ALCOHOL) LIQUID [PUNCH STUDIO, LLC]	5	Legacy NDC, 2 package rows	20220113_b1aa83ed-c721-6239-e053-2a95a90a7e7c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

Cleanslate
ALCOHOL
GLYCERIN
AMINOMETHYLPROPANOL
WATER
ALOE VERA LEAF
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
PROPYLENE GLYCOL
ALPHA-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75601-1004	75601-1004-1, 75601-1004-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ALPHA-TOCOPHEROL ACETATE	9E8X80D2L0	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d56f8ec0-0dab-b4a2-e053-2a95a90a7437			b1aa83ed-c721-6239-e053-2a95a90a7e7c	2022-01-12	Warnings	Exact identifier spl id: d56f8ec0-0dab-b4a2-e053-2a95a90a7437 spl set id: b1aa83ed-c721-6239-e053-2a95a90a7e7c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.