C-TIZERS 99.9- ethyl alcohol, isopropyl alcohol gel

C-tizers 99.9 by

Drug Labeling and Warnings

C-tizers 99.9 by is a Otc medication manufactured, distributed, or labeled by TIZER KOZMETIK LIMITED SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                 Purpose

Ethyl Alcohol 60% v/v........................    Antiseptic

Isopropyl Alcohol 10% v/v..................    Antiseptic

PURPOSE

Uses

Antibacterial Hand Sanitizer.

Warnings

Flammable, Keep away from eyes.

KEEP OUT OF REACH OF CHILDREN

Directions

Tear a single use pack of C-Tizers 99.9% and gently squeeze the full sachet onto your hands. Slowly rub your hands, covering the whole surface area until they are fully dry. No need to rinse at all afterwards.

Inactive ingredients

2,2,2-Nitrilotri(ethan-1-ol), Glycerin, Aloe vera extract, (2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-1-benzopyran-6-ol, CarboxyvinylPolymer, B.OCEAN 345276, C.I.:42090, Water.

Product label

INGREDIENTS AND APPEARANCE

C-TIZERS 99.9 
ethyl alcohol, isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80637-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	10 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80637-001-01	1.5 mL in 1 POUCH; Type 0: Not a Combination Product	10/06/2020
2	NDC: 80637-001-02	1.5 mL in 1 PACKET; Type 0: Not a Combination Product	10/06/2020
3	NDC: 80637-001-03	3 mL in 1 POUCH; Type 0: Not a Combination Product	10/06/2020
4	NDC: 80637-001-04	3 mL in 1 PACKET; Type 0: Not a Combination Product	10/06/2020
5	NDC: 80637-001-05	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2020
6	NDC: 80637-001-06	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2020
7	NDC: 80637-001-07	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2020
8	NDC: 80637-001-08	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2020
9	NDC: 80637-001-09	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2020
10	NDC: 80637-001-10	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2020
11	NDC: 80637-001-11	150000 mL in 1 DRUM; Type 0: Not a Combination Product	10/06/2020
12	NDC: 80637-001-12	45 mL in 1 POUCH; Type 0: Not a Combination Product	10/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/06/2020

Labeler - TIZER KOZMETIK LIMITED SIRKETI (595844669)

Establishment
Name	Address	ID/FEI	Business Operations
TIZER KOZMETIK LIMITED SIRKETI		595844669	manufacture(80637-001)