DOCTORS KLINE AND GREEN BOARD CERTIFIED DERMATOLOGIST HAND SANITIZER- alcohol gel

Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer by

Drug Labeling and Warnings

Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Formulated Solutions, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl alcohol 77% v/v

Purpose

Antiseptic

Uses

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

Warnings

For external use only:hands

Flammable, keep away from fire or flame.

When using this product

• 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

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

Keep out of reach of children.

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

Directions

• 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

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

Inactive ingredients

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

Package Labeling:

INGREDIENTS AND APPEARANCE

DOCTORS KLINE AND GREEN BOARD CERTIFIED DERMATOLOGIST HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 23667-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	77 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 23667-103-00	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/09/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/09/2021

Labeler - Formulated Solutions, LLC (143266687)

Establishment
Name	Address	ID/FEI	Business Operations
Formulated Solutions, LLC		143266687	manufacture(23667-103)