MOSAIC BATH AND SPA ANTIBACTERIAL WIPES- benzalkonium chloride cloth

Mosaic Bath and Spa Antibacterial Wipes by

Drug Labeling and Warnings

Mosaic Bath and Spa Antibacterial 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]

Drug Facts

Active Ingredient

Benzalkonium chloride 0.1%

Purpose

Antibacterial

Use

Hand sanitizer to help reduce bacteria on the skin

Warnings

For external use only

When using this product

do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or rash appears and lasts

Keep out of the reach of children.

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

Directions

• Wet hands thoroughly with product and allow to dry
• Discard wipes in trash receptacle after use. Do not flush
• Children under 6 years of age should be supervised when using this product

Inactive ingredients

Ethylhexylglycerin, Glycerin, Phenoxyethanol, Polyaminopropyl biguanide, Propylene Glycol, Purified water

Package Labeling: 50 wipes

Package Labeling: 70 wipes

INGREDIENTS AND APPEARANCE

MOSAIC BATH AND SPA ANTIBACTERIAL WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74934-021
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74934-021-01	50 in 1 BAG	06/20/2020	01/31/2026
1		3.78 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 74934-021-02	70 in 1 BAG	06/20/2020	01/31/2026
2		3.78 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)	06/20/2020	01/31/2026

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