WIPE THOSE HANDS- benzalkonium chloride cloth

Wipe Those Hands by

Drug Labeling and Warnings

Wipe Those Hands by is a Otc medication manufactured, distributed, or labeled by Mighty Good Solutions, LLC, Jiangsu Xiaolikang Medical Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Use

For hand sanitizing to decrease bacteria on the skin.

Warnings

For external use only.

When using this product

avoid contact with the eyes. In case of contact, flush eyes thoroughly with water.

Stop use and ask a doctor if

irritation and redness develop and persist.

Keep out of reach of children.

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

Directions

• Take wipe from pouch and rub thoroughly over all surfaces of both hands.
• Rub hands together briskly to dry.
• Supervise children under 6 years of age when using this product.
• Dispose of wipe.

Inactive ingredients

Ethylhexylglycerin, Glycerin, Phenoxyethanol, Propylene Glycol, Purified Water.

Questions or comments?

Call +1 (401) 307-1925

78091-250-04

78091-250-03

Package Labeling:

Package Labeling:30 Count

Package Labeling:40 Count

INGREDIENTS AND APPEARANCE

WIPE THOSE HANDS 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78091-251
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)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78091-251-04	10 in 1 POUCH	07/15/2023
1		1 in 1 PACKET
1		4.05 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 78091-251-03	42 in 1 POUCH	07/15/2023
2		4.05 mL in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 78091-251-02	20 in 1 POUCH	04/02/2025
3		4.05 mL in 1 APPLICATOR; Type 0: Not a Combination Product
4	NDC: 78091-251-05	30 in 1 POUCH	07/15/2023
4		4.05 mL in 1 PACKET; Type 0: Not a Combination Product
5	NDC: 78091-251-06	40 in 1 POUCH	07/15/2023
5		4.05 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/15/2023

Labeler - Mighty Good Solutions, LLC (029982731)

Registrant - Mighty Good Solutions, LLC (029982731)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangsu Xiaolikang Medical Technology Co., Ltd.		554546867	manufacture(78091-251)