PROSILK HAND SANITIZER- alcohol gel

Prosilk hand Sanitizer by

Drug Labeling and Warnings

Prosilk hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by DIAMO KOZMETIK SANAYI IC VE DIS TICARET LIMITED SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Ethyl Alcohol, 70%..................

Purpose

Antiseptic

Use

Flammable . keep away from sources of ignition-no smoking.

Warnings

for external use only.

Uses

In cases of contact with eyes, wash immediately.

Do not innhale or ingest.

Avoid contct with beoken skin.

KEEP OUT OF REACH OF CHILDREN

In cases of accidental ingestion,seek medical advice immediately. 

Keepaway from food sources.

Directions

Wet hands thoroughly with product and rub until dry without wiping.

Use without water.

Inactive Ingredients

Alcohol,Aqua,Glycerin,trinethanolamine,Acrylates/C10-30 Alkyl Acrylare Crosspolymer, Parfum, Aloe Barbadensis Leaf Juice,HexylCinnamal, 

Geraniol,Butypheny methlypropinal, Linalool, Limonene.

Please see label on the container.

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROSILK HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78242-001
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
LIMONENE, (+/-)- (UNII: 9MC3I34447)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78242-001-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2020
2	NDC: 78242-001-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/19/2020

Labeler - DIAMO KOZMETIK SANAYI IC VE DIS TICARET LIMITED SIRKETI (504571389)