INOVAKER LAB HAND SANITIZER- isopropyl alcohol gel

Inovaker Lab Hand Sanitizer by

Drug Labeling and Warnings

Inovaker Lab Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by UH Group LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Isopropyl alcohol 75% v/v

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin.

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.

Stop use and ask a doctor if

irritation or rash appears and lasts.

Keep out of reach of children.

If swalowed, get medical help or contact a Poison Control Center Right away.

Directions

-Place product on hands - Rub until dry

Inactive ingredients

WATER (AQUA), GLYCERIN, TRIETHANOLAMINE, CARBOMER, FRAGRANCE.

Package Labeling:60ml

Package Labeling:120ml

Package Labeling:250ml

Package Labeling:500ml

Package Labeling:4L

INGREDIENTS AND APPEARANCE

INOVAKER LAB HAND SANITIZER 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78106-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78106-002-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/24/2020
2	NDC: 78106-002-07	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/24/2020
3	NDC: 78106-002-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/24/2020
4	NDC: 78106-002-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/24/2020
5	NDC: 78106-002-06	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/24/2020

Labeler - UH Group LLC (025029589)