Hand Sanitizer Wipes by KYNC Design LLC Hand Sanitizer Wipes

Hand Sanitizer Wipes by

Drug Labeling and Warnings

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

Drug Details [pdf]

HAND SANITIZER WIPES- juniper clean 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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Hand Sanitizer Wipes

SPL UNCLASSIFIED SECTION

Active Ingredient(s)

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

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

Do not use if you are allergic to any of the ingeredients.

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.

If swallowed, get medical help or contact a Poison Control Center immediately.

Stop use and ask a doctor if irritation or rash occurs.

Keep out of reach of children.

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.

Other information

n/a

Inactive ingredients

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

Package Label - Principal Display Panel

110 mL NDC: 76557-001-01

245 mL NDC: 76557-001-01

HAND SANITIZER WIPES 
juniper clean cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76557-001
Route of Administration	CUTANEOUS, 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
CLOVE (UNII: K48IKT5321)
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: 76557-001-02	245 mg in 1 CANISTER; Type 0: Not a Combination Product	07/11/2020
2	NDC: 76557-001-01	110 mg in 1 CANISTER; Type 0: Not a Combination Product	07/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/10/2020	11/30/2022

Labeler - KYNC Design LLC (039933298)

Revised: 11/2022

Document Id: ee4d2a97-1f88-e18f-e053-2995a90aaaa6

34390-5

Set id: a5279159-e2f4-e402-e053-2a95a90af50e

Version: 4

Effective Time: 20221125