NOVAGEL HAND SANITIZER- antiseptic gel gel

Hydra Pearl Liquid by

Drug Labeling and Warnings

Hydra Pearl Liquid by is a Otc medication manufactured, distributed, or labeled by PlasmaDent Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Nova Gel

Advanced Hand Sanitizer

Original Scent

Leaves Hands Feeling Soft

8 FL OZ (236.6 mL)

Active Ingredient

Active Ingredient Purpose

Ethyl Alcohol 70% v/v ----------------Antiseptic

Purpose

Use- To decrease bacteria on the skin

Use

Use-To decrease bacteria on the skin

Keep out of the reach of children

Keep out of the reach of children

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.

Other information

Other information- Do not store above 110 oF (43 oC)

May discolor some fabrics.

Harmful to wood finishes and plastics

Inactive Ingredient Section

Inactive Ingredient- Water, Glycerin, Carbomer, Aminomethyl propanol, fragrance

INGREDIENTS AND APPEARANCE

NOVAGEL HAND SANITIZER 
antiseptic gel gel

Product 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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - PlasmaDent Inc (053111649)