Hand 2 Mind Alcohol-Free Sanitizing Wet Wipes

Hand 2 Mind Alcohol-Free Sanitizing Wet Wipes by

Drug Labeling and Warnings

Hand 2 Mind Alcohol-Free Sanitizing Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Zhejiang iColor Biotech Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND 2 MIND ALCOHOL-FREE SANITIZING WET WIPES- benzalkonium chloride cloth 
Zhejiang iColor Biotech Co., Ltd

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Hand 2 Mind Alcohol-Free Sanitizing Wet Wipes

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use(s):

For use when soap and water are not available.

Warnings

For external use only.

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash occurs.These may be signs of a serious condition.

Keep out of reach of children.

lf swallowed, get medical help or contact a Poison Control Center right away.

Directions:

Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store in a cool, dry area.·Keep container closed when not in use.·Dispose of used wipes in a trash bin.Do not flush.

Inactive ingredients 

●Water, Fragrance,Citric Acid,Propylene Glycol,Polyoxyethylene Alkyl Ether,Diazolidinyl Urea, Iodopropyny1 Butylcarbamate.

Package Labeling

HAND 2 MIND ALCOHOL-FREE SANITIZING WET WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74934-051
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
LAURETH-12 (UNII: OAH19558U1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74934-051-10	10 in 1 BAG	09/15/2020	01/31/2026
1		3.1 mL 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 Drug	505G(a)(3)	09/15/2020	01/31/2026

Labeler - Zhejiang iColor Biotech Co., Ltd (554528308)

Revised: 1/2024

Document Id: 0fb3cf9b-c1d4-4a5c-e063-6294a90a83ee

34390-5

Set id: af8401fd-d5b3-4a1e-e053-2995a90ab299

Version: 2

Effective Time: 20240124