Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer Antiseptic

Manufacturer: Formulated Solutions, LLC
Effective date: 2023-11-30
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:03:03

Label at a glance#

ProductDoctors Kline and Green Board Certified Dermatologist Hand Sanitizer Antiseptic

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Hold can upside down and dispense into palm. Place enough product on hands to cover all surfaces. Rub hands together until dry Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses(s)

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Extermely flammable, do not use near heat or flame or while smoking.

Do not use

OTC - DO NOT USE SECTION

On children less than 2 months of age
On open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth
In case of contact with eyes, rinse eyes thoroughly with water.
Do not puncture or incinerate
Contents under pressure
Do not expose to heat or store at temperature above 120°F (49°C)

Stop use and ask a doctor

OTC - STOP USE SECTION

If irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Hold can upside down and dispense into palm. Place enough product on hands to cover all surfaces. Rub hands together until dry
Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Hydrofluorocarbon 152a; Isobutane; Emulsifying Wax NF; Propane

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616763	ethanol 62 % Topical Foam	PSN	2
616763	ethanol 0.62 ML/ML Topical Foam	SCD	2
616763	ethanol 62 % Topical Foam	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
23667-104-00	Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer Antiseptic	222 mL in 1 CAN	AEROSOL, FOAM	222		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
23667-104	DOCTORS KLINE AND GREEN BOARD CERTIFIED DERMATOLOGIST HAND SANITIZER ANTISEPTIC (ALCOHOL) AEROSOL, FOAM [FORMULATED SOLUTIONS, LLC]	2	Legacy NDC, 1 package rows	20231201_bc7e624c-0ee4-b6b5-e053-2a95a90abf8d.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer Antiseptic
ALCOHOL
WATER
1,1-DIFLUOROETHANE
ISOBUTANE
PROPANE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
23667-104	23667-104-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
1,1-DIFLUOROETHANE	0B1U8K2ME0	IACT
ISOBUTANE	BXR49TP611	IACT
PROPANE	T75W9911L6	IACT
ALCOHOL	3K9958V90M	ACTIB

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
5657471a-9573-6ccd-e063-6294a90a1044			bc7e624c-0ee4-b6b5-e053-2a95a90abf8d	2026-07-11	Warnings	Exact identifier spl set id: bc7e624c-0ee4-b6b5-e053-2a95a90abf8d

Reported adverse events (FAERS/openFDA)#

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