DR.OSLER HAND SANITIZER- alcohol gel

Dr.Osler HAND SANITIZER by

Drug Labeling and Warnings

Dr.Osler HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Corelandmark Inc., AD Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol

INACTIVE INGREDIENT

Water, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Butylene Glycol, Triethanolamine, Aloe Barbadensis Leaf Extract, Eucalyptus Globulus Leaf Extract, Glycerin, 1,2-Hexanediol, Ethylhexylglycerin, Carbomer, Fragrance

PURPOSE

Antiseptic

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

For the external use only

WARNINGS

For external use only.

Flammable, keep away from fire or flame.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Put enough amount in your palm and rub hands together until dry. Children under 6 years of age should be supervised by adult who is older than 21 years of age.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.OSLER HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78050-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	175 mL  in 250 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78050-0001-1	250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

Labeler - Corelandmark Inc. (688505535)

Registrant - Corelandmark Inc. (688505535)

Establishment
Name	Address	ID/FEI	Business Operations
AD Cosmetics Co., Ltd.		688155662	manufacture(78050-0001)

Establishment
Name	Address	ID/FEI	Business Operations
Corelandmark Inc.		688505535	label(78050-0001)