HAND SANITIZER GEL BIOKAAB- ethyl alcohol, citrus extracts gel SANIDEP ADVANCED SANITIZER WITH ORGANIC EXTRACTS- organic citric filipherina extracts, benzalkonium chloride liquid HAND SANITIZER BIOKAAB- organic citric filipherina extracts, benzalkonium chloride liquid DEQGEL ADVANCED HAND SANITIZER- ethyl alcohol, citrus extracts gel

DEQGEL Advanced Hand Sanitizer by

Drug Labeling and Warnings

DEQGEL Advanced Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Biokaab Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Dossage and Administration

Place enough product on hands to cover all surfaces. Rub hands to get her until dry.

Indications

Place enough product on hands to cover all surfaces. Rub hands to get her until dry.

Warnings

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use
in 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.

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.

Inactive Ingedients

Inactive ingredients, Poly acrylic acid, glycerin, purified water USP

KEEP OUT OF REACH OF CHILDREN

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

Active Ingredients

Active ingredient[s] Purpose

• Ethyl Alcohol 96 o 60%......................................................................................................................................................Antiseptic
• Citric Oil Extracts 1%.........................................................................................................................................................Antiseptic
• Chlorhexidine Gluconate 1%.............................................................................................................................................Antiseptic

​

Purpose

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

Active ingredient[s] Purpose

Ethyl Alcohol 96o 60% ……………….....................................................................................................................................Antiseptic

Citric Oil Extracts 1% ..............................................................................................................................................................Antiseptic

Chlorhexidine Gluconate 1%...................................................................................................................................................Antiseptic

LABEL

SANIDEP ADVANCED SANITIZER LABEL

HAND SANITIZER GEL LABEL

SANIDEP LABEL

DEQ GEL ANTIBACTERIAL GEL

DEQ GEL Antibacterial Gel

DEQ GEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER GEL  BIOKAAB
ethyl alcohol, citrus extracts gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74155-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	600 mg  in 1 mL
GRAPEFRUIT OIL (UNII: YR377U58W9) (GRAPEFRUIT OIL - UNII:YR377U58W9)	GRAPEFRUIT OIL	10 mg  in 1 mL
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	375 mg  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	5 mg  in 1 mL
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)	6 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74155-101-07	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
2	NDC: 74155-101-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
3	NDC: 74155-101-38	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
4	NDC: 74155-101-20	200000 mL in 1 DRUM; Type 0: Not a Combination Product	04/01/2020
5	NDC: 74155-101-19	20000 mL in 1 DRUM; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/20/2020

SANIDEP ADVANCED SANITIZER WITH ORGANIC EXTRACTS 
organic citric filipherina extracts, benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74155-211
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	120 g  in 1 L
GRAPEFRUIT OIL (UNII: YR377U58W9) (GRAPEFRUIT OIL - UNII:YR377U58W9)	GRAPEFRUIT OIL	150 g  in 1 L
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	50 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 20 (UNII: 7T1F30V5YH)	10 g  in 1 L
WATER (UNII: 059QF0KO0R)	690 g  in 1 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74155-211-08	0.24 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/30/2020
2	NDC: 74155-211-07	0.6 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/30/2020
3	NDC: 74155-211-38	3.785 L in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 74155-211-20	200 L in 1 DRUM; Type 0: Not a Combination Product	03/30/2020
5	NDC: 74155-211-19	20 L in 1 DRUM; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/20/2020

HAND SANITIZER  BIOKAAB
organic citric filipherina extracts, benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74155-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	120 mg  in 1 mL
GRAPEFRUIT OIL (UNII: YR377U58W9) (GRAPEFRUIT OIL - UNII:YR377U58W9)	GRAPEFRUIT OIL	150 mg  in 1 mL
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 20 (UNII: 7T1F30V5YH)	10 mg  in 1 mL
WATER (UNII: 059QF0KO0R)	690 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74155-111-08	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/30/2020
2	NDC: 74155-111-07	50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/30/2020
3	NDC: 74155-111-38	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 74155-111-20	200000 mL in 1 DRUM; Type 0: Not a Combination Product	03/30/2020
5	NDC: 74155-111-19	20000 mL in 1 DRUM; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/20/2020

DEQGEL ADVANCED HAND SANITIZER 
ethyl alcohol, citrus extracts gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74155-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	600 mg  in 1 mL
GRAPEFRUIT OIL (UNII: YR377U58W9) (GRAPEFRUIT OIL - UNII:YR377U58W9)	GRAPEFRUIT OIL	10 mg  in 1 mL
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	375 mg  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	5 mg  in 1 mL
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)	6 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74155-201-38	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
2	NDC: 74155-201-20	200000 mL in 1 DRUM; Type 0: Not a Combination Product	04/01/2020
3	NDC: 74155-201-19	20000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/20/2020

Labeler - Biokaab Inc (117455364)