HAND2MIND SANITIZING WET WIPES- benzalkonium chloride solution

hand2mind Sanitizing Wet Wipes by

Drug Labeling and Warnings

hand2mind Sanitizing Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Taizhou Duorui Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

For use when soap and water are not available

Warnings

For external use only.

When using this product, keep out of eyes, ears or 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

Keep out of reach of children. If swallowed, get immediate 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 trash bin. Do not flush.

Inactive ingredients

Water, Fragrance, Citric Acid, Propylene Glycol, Polyoxyethylene Alkyl Ether, Diazolidinyl Urea, Iodopropynyl Butylcarbamate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND2MIND SANITIZING WET WIPES 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80800-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80800-002-01	1 in 1 PACKAGE	03/12/2021
1		3.46 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 80800-002-02	10 in 1 PACKAGE	03/12/2021
2		3.46 mL in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 80800-002-03	20 in 1 PACKAGE	03/12/2021
3		3.46 mL in 1 APPLICATOR; Type 0: Not a Combination Product
4	NDC: 80800-002-04	30 in 1 PACKAGE	03/12/2021
4		3.46 mL in 1 APPLICATOR; Type 0: Not a Combination Product
5	NDC: 80800-002-05	60 in 1 PACKAGE	03/12/2021
5		3.46 mL in 1 APPLICATOR; Type 0: Not a Combination Product
6	NDC: 80800-002-06	110 in 1 PACKAGE	03/12/2021
6		3.46 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/12/2021

Labeler - Taizhou Duorui Biotechnology Co., Ltd. (713362289)

Establishment
Name	Address	ID/FEI	Business Operations
Taizhou Duorui Biotechnology Co., Ltd.		713362289	manufacture(80800-002)