Evident Clean Hand Sanitizing Wipes

Evident Clean Hand Sanitizing Wipes by

Drug Labeling and Warnings

Evident Clean Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by KYNC Design LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

EVIDENT CLEAN HAND SANITIZING WIPES- hand sanitizing wipes cloth 
KYNC Design 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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Evident Clean Hand Sanitizing Wipes

SPL UNCLASSIFIED SECTION

Active Ingredient(s)

Benzalkonium Chloride (CAS NO: 68424-85-1), 0.125% .

Purpose

Antimicrobial

Use

Hand sanitizing wipes help remove bacteria from hands and kill 99.99% of germs. Removes dirt to help with health and cleanliness.

WARNINGS

Use on hands only.

Do not use

If you are allergic to any of the ingredients.

Stop use and ask a doctor

if irritation or rash occurs.

Do not use in or near the eyes.

If contact occurs rinse with plenty of water. Remove contact lenses, if present and easy to do. Continue rinsing. If eye irritation persists, get medical advice/attention.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center immediately.

Directions

To Open Package: Flip open dispensing cap. Locate wipe at center of roll and pull through small openning in lid. For best results dispense wipes at an angle. Wet hands thoroughly with product and allow to dry. When finished, snap lid cap shut to retain moisture. Discard wipe in trash receptacle after use. Do not flush.

Inactive ingredients

Water(Aqua), Ethanol, Decyl Glucoside, Glycerine, Aloe Vera Extract, D-Panthenol, Fragrance (Perfume)

Package Label - Principal Display Panel

Evident Clean 35ct

NDC: 76557-200-01

Evident Clean 75ct

NDC: 76557-200-02

EVIDENT CLEAN HAND SANITIZING WIPES 
hand sanitizing wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76557-200
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.125 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
DEXPANTHENOL (UNII: 1O6C93RI7Z)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76557-200-02	75 in 1 CANISTER	06/04/2020
1		3.14 mg in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 76557-200-01	35 in 1 CANISTER	06/04/2020
2		3.14 mg in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3	NDC: 76557-200-03	72 in 1 PACKAGE	06/04/2020
3		3.14 mg in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/04/2020	05/20/2022

Labeler - KYNC Design LLC (039933298)

Revised: 5/2022

Document Id: df758635-d08e-27ae-e053-2995a90a8854

34390-5

Set id: aa7d6948-60cd-342d-e053-2a95a90a42b0

Version: 4

Effective Time: 20220520