Juniper Clean 72% Alcohol Wipes by Kync Design LLC 72% Alcohol Wipe

Juniper Clean 72% Alcohol Wipes by

Drug Labeling and Warnings

Juniper Clean 72% Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by Kync Design LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

JUNIPER CLEAN 72% ALCOHOL WIPES- 72% alcohol wipe 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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72% Alcohol Wipe

Active Ingredient(s)

Isopropyle Alcohol 72%, Benzalkonium Chloride .125%.

Purpose

Antimicrobial.

Use

Hand sanitizing wipes help remove bacteria from hands and kill 99.9% of germs. Removes dirt to help with health and cleanliness.

Warnings

Use on hands only. Flammable. Keep away from heat or flame.

Do not use

if you are allergic to any of the ingredients.

Avoid Contact with eyes

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



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

Stop use and ask a doctor

if irritation or rash occurs.

Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.

Directions

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. When finished snap lid cap shut to retain moisture.

Do not flush. Dispose of wipe in trash after use. Do not reuse or refill this contained; discard in trash.

Other information

Store between 15-30C (59-86F)

Inactive ingredients

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

Package Label - Principal Display Panel

JUNIPER CLEAN 72% ALCOHOL WIPES 
72% alcohol wipe cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76557-005
Route of Administration	CUTANEOUS, TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	72 mg  in 100 mg
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)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76557-005-03	147 mg in 1 CANISTER; Type 0: Not a Combination Product	08/05/2020
2	NDC: 76557-005-04	106 mg in 1 PACKAGE; Type 0: Not a Combination Product	08/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/01/2020	05/20/2022

Labeler - Kync Design LLC (039933298)

Revised: 5/2022

Document Id: df755bff-6bda-678e-e053-2a95a90a15cf

34390-5

Set id: ac26f7df-538b-5b87-e053-2995a90aab86

Version: 4

Effective Time: 20220520