INOVAKER LAB HAND SANITIZER- isopropyl 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

Bottle

Package Labeling:120ml

Bottle2

Package Labeling:250ml

Bottle3

Package Labeling:500ml

Bottle4

Package Labeling:4L

Bottle5

INOVAKER LAB HAND SANITIZER 
isopropyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78106-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.75 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78106-002-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product07/24/2020
2NDC:78106-002-07120 mL in 1 BOTTLE; Type 0: Not a Combination Product07/24/2020
3NDC:78106-002-02250 mL in 1 BOTTLE; Type 0: Not a Combination Product07/24/2020
4NDC:78106-002-03500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/24/2020
5NDC:78106-002-064000 mL in 1 BOTTLE; Type 0: Not a Combination Product07/24/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/24/2020
Labeler - UH Group LLC (025029589)

Revised: 7/2020
Document Id: ab6c4a4b-97a1-3631-e053-2a95a90a614a
Set id: eaf8dd8e-6cc6-4840-9668-eee3e69bbcc6
Version: 1
Effective Time: 20200727
 
UH Group LLC