Evident Clean Simple Wipes

Evident Clean Simple Wipes by

Drug Labeling and Warnings

Evident Clean Simple 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 SIMPLE WIPES- hand cleaning 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 Simple Wipes

Active Ingredient(s)

Benzalkonium Chloride (CAS NO: 68424-85-1), 0.25% .

Purpose

Antimicrobial

Use

Hand cleaning wipes.

WARNINGS

Use on hands.

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 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, Isopropyl Alcohol, Sodium Benzoate and Potasium Sorbate and Cetrimonium Chloride, DDAC, Caprylyl/Decyl Glucoside, Polymer, E.D.T.A, Fragrance (Perfume)

Simple Device Cleaning Wipes Flowpack 25 ct

Simple Device Cleaning Wipes Flowpack 50 ct

EVIDENT CLEAN SIMPLE WIPES 
hand cleaning wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76557-201
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 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
SODIUM BENZOATE (UNII: OJ245FE5EU)
MCC-950 SODIUM SALT (UNII: 66BL55B687)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
TRIMETHYLENEDIAMINETETRAACETIC ACID (UNII: 3F6OA94EER)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76557-201-02	50 in 1 PACKAGE	10/15/2020	05/20/2022
1		4.4 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 76557-201-01	25 in 1 PACKAGE	10/15/2020	05/20/2022
2		4.4 g 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	10/15/2020	05/20/2022

Labeler - KYNC Design LLC (039933298)

Revised: 5/2022

Document Id: df757765-586f-0fd2-e053-2a95a90a5843

34390-5

Set id: b1ae60cc-8cc7-741e-e053-2a95a90a1aff

Version: 3

Effective Time: 20220520