KMF Hand Sanitizer Cleansing Gel

KMF Hand Sanitizer Cleansing Gel by

Drug Labeling and Warnings

KMF Hand Sanitizer Cleansing Gel by is a Otc medication manufactured, distributed, or labeled by Cemi International, Inc, HPPE, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KMF HAND SANITIZER CLEANSING GEL- isopropyl alcohol gel 
Cemi International, Inc

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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KMF Hand Sanitizer Cleansing Gel

Drug Facts

Active ingredient

Isopropyl alcohol 75% v/v

Purpose

Antiseptic

Uses ● hand sanitizer to decrease bacteria on the skin ● recommended for repeated use ● for use when soap and water are not available

Warnings

Flammable, keep away from fire/flame

For external use only

Do not use ● in children less than 2 months of age ● on open skin wounds

When using this product ● do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

• irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions ● wet hands thoroughly with product and allow to dry without wiping ● supervise children under 6 years of age when using this product to avoid swallowing

Other information● store between 15-30°C (59-86°F) ● avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients  glycerin,hydrogen peroxide, hydroxypropyl methylcellulose, water

Questions? +1-800-822-4320
You may also report serious side effects to this phone number.
Mon-Fri 9:00 AM - 5:00 PM

75% ALCOHOL

SCENT FREE

ANTISEPTIC GEL
MOISTURIZING FORMULA

310K5180601

Distributed by: Windmill Health Products, LLC, West Caldwell, NJ 07006

©KMF IP Holdings, LLC  All rights reserved.

kissmyface.com

N11999

Packaging

KMF HAND SANITIZER CLEANSING GEL 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73741-115
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73741-115-02	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/30/2020	07/06/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/30/2020	07/06/2022

Labeler - Cemi International, Inc (015038336)

Establishment
Name	Address	ID/FEI	Business Operations
HPPE, LLC		078769356	manufacture(73741-115)

Revised: 11/2022

Document Id: 4907e4e3-c300-4488-832b-e066002066b4

34390-5

Set id: e086b9a0-a7f1-477e-ace3-e178f7334fd2

Version: 2

Effective Time: 20221116