Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer

Manufacturer: Formulated Solutions, LLC
Effective date: 2023-11-29
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

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 77% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only:hands

Flammable, keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. In case of contact with eyes, flush thoroughly with water.
avoid contact with broken skin
do not inhale or ingest

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develop
condition persists for more than 72 hours

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

wet hands thoroughly with product and allow to dry without wiping
for children under 6, use only under adult supervision
not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

do not store above 110°F (43°C)
may discolor some fabrics or surfaces
harmful to wood finished and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ammonium Acryloyldimethyltaurate/VP Copolymer, Caprylic/ Capric Triglyceride, HYdroxyethyl Urea, Tocopheryl Acetate, Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1788839	ethanol 77 % Topical Gel	PSN	2
1788839	ethanol 0.77 ML/ML Topical Gel	SCD	2
1788839	ethanol 77 % Topical Gel	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
23667-103-00	Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer	50 mL in 1 BOTTLE	GEL	50		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
23667-103	DOCTORS KLINE AND GREEN BOARD CERTIFIED DERMATOLOGIST HAND SANITIZER (ALCOHOL) GEL [FORMULATED SOLUTIONS, LLC]	2	Legacy NDC, 1 package rows	20231201_bc7d5a84-53b6-0d76-e053-2a95a90ade8c.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer
ALCOHOL
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
MEDIUM-CHAIN TRIGLYCERIDES
HYDROXYETHYL UREA
.ALPHA.-TOCOPHEROL ACETATE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
23667-103	23667-103-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER	W59H9296ZG	IACT
MEDIUM-CHAIN TRIGLYCERIDES	C9H2L21V7U	IACT
HYDROXYETHYL UREA	MBQ7DDQ7AR	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
WATER	059QF0KO0R	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
56573f0f-06c3-7209-e063-6394a90a6b23			bc7d5a84-53b6-0d76-e053-2a95a90ade8c	2026-07-11	Warnings	Exact identifier spl set id: bc7d5a84-53b6-0d76-e053-2a95a90ade8c

Reported adverse events (FAERS/openFDA)#

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