Label: 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
-
Contains inactivated NDC Code(s)
NDC Code(s): 74155-101-07, 74155-101-08, 74155-101-19, 74155-101-20, view more74155-101-38, 74155-111-07, 74155-111-08, 74155-111-19, 74155-111-20, 74155-111-38, 74155-201-03, 74155-201-19, 74155-201-20, 74155-201-38, 74155-211-04, 74155-211-07, 74155-211-08, 74155-211-19, 74155-211-20, 74155-211-38 - Packager: Biokaab Inc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 20, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
NDC 74155-202 DEQGEL ADVANCED HAND SANITIZER GEL LABEL
HAND SANITIZER GEL LABEL
DEQGEL Hand Sanitizer Gel Active Ingredients
Active ingredient[s] Purpose
- Ethyl Alcohol 96 o 60%......................................................................................................................................................Antiseptic
- Citric Oil Extracts 1%.........................................................................................................................................................Antiseptic
- Chlorhexidine Gluconate 1%.............................................................................................................................................Antiseptic
DEQGEL Dossage and Administration
Place enough product on hands to cover all surfaces. Rub hands to get her until dry.
Hand Sanitizer Gel 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 woundsWhen 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.HandSanitizerGel
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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
-
NDC 74155-211 SANIDEP Alcohol Free Hand Sanitizer
SANIDEP ALCOHOL FREE HAND SANITIZER
For external use only. NON Flammable.
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.SANIDEP Active Ingredients
Benzalkonium Choride 10% ........................................................................................................................................................Antiseptic
Citric Extracts 15% ......................................................................................................................................................................Antiseptic
Chlorhexidine Gluconate 5% .......................................................................................................................................................Antiseptic
INSTRUCTIONS SANIDEP
Place enough product on hands to cover all surfaces. Rub hands to get her until dry.
KEEP OUT OF CHILDREN
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Supervise children under 6years of age when using this product to avoid swallowing.
Purpose
Active ingredient[s] Purpose
Benzalkonium Choride 10% ........................................................................................................................................................Antiseptic
Citric Extracts 15% ......................................................................................................................................................................Antiseptic
Chlorhexidine Gluconate 5% .......................................................................................................................................................Antiseptic
Use[s]
Health care personnel hand rub to help reduce bacteria that potentially can cause disease.
-
INGREDIENTS AND APPEARANCE
HAND SANITIZER GEL BIOKAAB
ethyl alcohol, citrus extracts gelProduct 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 liquidProduct 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 6 NDC:74155-211-04 0.125 L in 1 BOTTLE, SPRAY; 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 liquidProduct 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 gelProduct 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 4 NDC:74155-201-03 100 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 Labeler - Biokaab Inc (117455364)