Label: HYDRA PEARL HAND SANITIZER- antiseptic gel gel
NOVAGEL HAND SANITIZER- antiseptic gel gel
IVOGEL HAND SANITIZER- antiseptic gel gel
HYDRA PEARL LIQUID- sanitizing hand spray liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73893-001-01, 73893-001-02, 73893-001-03, 73893-001-04, view more73893-001-05, 73893-001-06, 73893-001-07, 73893-001-08, 73893-001-09, 73893-001-10, 73893-001-11, 73893-001-12, 73893-002-02, 73893-002-03, 73893-002-04, 73893-002-05, 73893-002-06, 73893-002-08, 73893-002-11, 73893-002-12, 73893-003-01, 73893-003-02, 73893-003-03, 73893-003-04, 73893-004-01, 73893-004-02, 73893-004-03, 73893-004-04, 73893-004-05, 73893-004-06, 73893-004-07, 73893-004-08, 73893-004-09, 73893-004-10, 73893-004-11, 73893-004-12 - Packager: PlasmaDent Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 February 25, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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Nova Gel
Advanced Hand Sanitizer
Original Scent
Leaves Hands Feeling Soft
8 FL OZ (236.6 mL)
Warnings
Warnings
Flammable. Keep away from fire or flame.
For external use only
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stope use and ask a doctor if irritation or rash appears and lasts.
Keep out of reach of children. If swallowed get medical help or contact a poisen control center right away.
Directions
Directions-wet hands thoroughly with product and allow to dry without wiping. For children under 6 use only under adult supervision. Not recommended for infants.
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INGREDIENTS AND APPEARANCE
HYDRA PEARL HAND SANITIZER
antiseptic gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73893-002 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 AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.1 g in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 2 g in 100 mL CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) 0.3 g in 100 mL WATER (UNII: 059QF0KO0R) 32.8 g in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73893-002-02 236.6 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 08/12/2020 2 NDC:73893-002-03 473.2 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 08/12/2020 3 NDC:73893-002-04 295.7 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 08/12/2020 4 NDC:73893-002-05 946.4 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 08/12/2020 5 NDC:73893-002-06 3800 mL in 1 CONTAINER; Type 0: Not a Combination Product 08/12/2020 6 NDC:73893-002-11 59.1 mL in 1 TUBE; Type 0: Not a Combination Product 08/12/2020 7 NDC:73893-002-08 18900 mL in 1 CONTAINER; Type 0: Not a Combination Product 10/02/2020 8 NDC:73893-002-12 189000 mL in 1 DRUM; Type 0: Not a Combination Product 02/28/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/12/2020 NOVAGEL HAND SANITIZER
antiseptic gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73893-001 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 AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.1 g in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 2 g in 100 mL CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) 0.3 g in 100 mL WATER (UNII: 059QF0KO0R) 32.8 g in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73893-001-01 59.1 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 03/30/2020 2 NDC:73893-001-02 236.6 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 03/30/2020 3 NDC:73893-001-03 473.2 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 04/06/2020 4 NDC:73893-001-04 295.7 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 04/15/2020 5 NDC:73893-001-05 946.4 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 04/15/2020 6 NDC:73893-001-06 3800 mL in 1 CONTAINER; Type 0: Not a Combination Product 04/15/2020 7 NDC:73893-001-07 9500 mL in 1 CONTAINER; Type 0: Not a Combination Product 04/15/2020 8 NDC:73893-001-08 18900 mL in 1 CONTAINER; Type 0: Not a Combination Product 04/15/2020 9 NDC:73893-001-09 113600 mL in 1 DRUM; Type 0: Not a Combination Product 04/15/2020 10 NDC:73893-001-10 189300 mL in 1 DRUM; Type 0: Not a Combination Product 04/15/2020 11 NDC:73893-001-11 59.1 mL in 1 TUBE; Type 0: Not a Combination Product 07/20/2020 12 NDC:73893-001-12 354.9 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 08/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/30/2020 IVOGEL HAND SANITIZER
antiseptic gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73893-004 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 AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.1 g in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 2 g in 100 mL CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) 0.3 g in 100 mL WATER (UNII: 059QF0KO0R) 32.8 g in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73893-004-01 59.1 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 10/23/2020 2 NDC:73893-004-02 236.6 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 10/23/2020 3 NDC:73893-004-03 473.2 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 10/23/2020 4 NDC:73893-004-04 295.7 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 10/23/2020 5 NDC:73893-004-05 946.4 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 10/23/2020 6 NDC:73893-004-06 3800 mL in 1 CONTAINER; Type 0: Not a Combination Product 10/23/2020 7 NDC:73893-004-07 9500 mL in 1 CONTAINER; Type 0: Not a Combination Product 10/23/2020 8 NDC:73893-004-08 18900 mL in 1 CONTAINER; Type 0: Not a Combination Product 10/23/2020 9 NDC:73893-004-09 113600 mL in 1 DRUM; Type 0: Not a Combination Product 10/23/2020 10 NDC:73893-004-10 189300 mL in 1 DRUM; Type 0: Not a Combination Product 10/23/2020 11 NDC:73893-004-11 59.1 mL in 1 TUBE; Type 0: Not a Combination Product 10/23/2020 12 NDC:73893-004-12 354.9 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 10/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/23/2020 HYDRA PEARL LIQUID
sanitizing hand spray liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73893-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 1.45 mL in 100 mL WATER (UNII: 059QF0KO0R) 18.55 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73893-003-01 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/09/2020 2 NDC:73893-003-02 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/09/2020 3 NDC:73893-003-03 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/09/2020 4 NDC:73893-003-04 227304 mL in 1 DRUM; Type 0: Not a Combination Product 02/28/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/09/2020 Labeler - PlasmaDent Inc (053111649)
