Inovaker Lab Hand Sanitizer

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]

INOVAKER LAB HAND SANITIZER- alcohol gel 
UH Group LLC

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.

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Inovaker Lab Hand Sanitizer

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

INOVAKER LAB HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78106-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	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: 78106-001-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2020	05/30/2020
2	NDC: 78106-001-07	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2020	05/30/2020
3	NDC: 78106-001-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2020	05/30/2020
4	NDC: 78106-001-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2020	05/30/2020
5	NDC: 78106-001-06	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2020	05/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/30/2020	05/30/2020

Labeler - UH Group LLC (025029589)

Revised: 7/2020

Document Id: ab6d0074-00ec-b0cf-e053-2a95a90a61d8

34390-5

Set id: c26ec256-aa54-492d-8413-6df744a40a3d

Version: 2

Effective Time: 20200727

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