D.THERAPINO HAND SANITIZER- alcohol gel

d.therapino Hand Sanitizer by

Drug Labeling and Warnings

d.therapino Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by David Cosmetic Co Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

alcohol

INACTIVE INGREDIENT

Water
Carbomer
Aloe Barbadensis Leaf Extract
Water
Butylene Glycol
1,2-Hexanediol
Triethanolamine
Menthol

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

PURPOSE

hand sanitizer to help reduce bacteria that potentially can cause disease

for use when soap and water are not available

INDICATIONS & USAGE

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.

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

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

D.THERAPINO HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58241-0003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
MENTHOL (UNII: L7T10EIP3A)
CARBOMER 940 (UNII: 4Q93RCW27E)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58241-0003-1	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/11/2020
2	NDC: 58241-0003-2	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/11/2020

Labeler - David Cosmetic Co Ltd (695697845)

Registrant - David Cosmetic Co Ltd (695697845)

Establishment
Name	Address	ID/FEI	Business Operations
David Cosmetic Co Ltd		695697845	manufacture(58241-0003) , label(58241-0003)