DOCTORS KLINE AND GREEN BOARD CERTIFIED DERMATOLOGIST HAND SANITIZER ALCOHOL ANTISEPTIC- alcohol liquid

Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer Alcohol Antiseptic by

Drug Labeling and Warnings

Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer Alcohol Antiseptic 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(s)

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

Warnings

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

Do not use

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

When using this product

• 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 temperatures above 120°F (49°C)

Stop use and ask a doctor

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

Keep out of reach of children.

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

Directions

• 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

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

Inactive ingredients

Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/VP Copolymer, HYdroxyethyl Urea, Tocopheryl Acetate, Water

Package Labeling:

INGREDIENTS AND APPEARANCE

DOCTORS KLINE AND GREEN BOARD CERTIFIED DERMATOLOGIST HAND SANITIZER ALCOHOL ANTISEPTIC 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 23667-102
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
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: 23667-102-00	166 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)