Cleansing Hand Sanitizer by Koh Gen Do / Inspec Solutions LLC Drug Facts

Cleansing Hand Sanitizer by

Drug Labeling and Warnings

Cleansing Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Koh Gen Do, Inspec Solutions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CLEANSING HAND SANITIZER- alcohol gel 
Koh Gen Do

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Drug Facts

Active ingredient                       Purpose

Ethyl Alcohol 62%                       Antimicrobial                         

Warnings

For extamaf use only.

Flammable. Keep away from fire or flame.

When using this product  keep oot of eyes. Rinse with water lo remove.
Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a Polson Control Center lmmediately.

Uses

Hand sanitizer to help reduce bacteria on the skin.

Directions

Place enough product on your palm to thoroughly cover your hands Rub hands together briskly until dry.

Other infonnation

store below 11 o· (43°C )

Inactive ingredients

Aminomethyl Propanol, Carbomer, Fragrance, Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Aloe, Water.

Questions?

1-877-754-3872

CLEANSING HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51668-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)	Â
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)	Â
GLYCERIN (UNII: PDC6A3C0OX)	Â
ISOPROPYL ALCOHOL (UNII: ND2M416302)	Â
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)	Â
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	Â
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	Â
WATER (UNII: 059QF0KO0R)	Â
ALOE (UNII: V5VD430YW9)	Â

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51668-007-03	118 mL in 1 TUBE; Type 0: Not a Combination Product	06/22/2020	12/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/22/2020	12/09/2025

Labeler - Koh Gen Do (020836160)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions LLC		081030372	manufacture(51668-007)

Revised: 12/2025

Document Id: 45c82030-fff6-3984-e063-6294a90abc03

34390-5

Set id: 5408fc2c-d09f-4b94-acb4-d4450e6964cb

Version: 9

Effective Time: 20251212

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