FDA.reportPublic FDA data

Mosaic Bath and Spa Antibacterial Wipes

Manufacturer
Anhui Yunzhiyu Daily Chemical Products Co., Ltd
Effective date
2020-10-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:09:47

Label at a glance#

ProductMosaic Bath and Spa Antibacterial Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

When using this product 

OTC - WHEN USING SECTION

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

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation or rash appears and lasts

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

INACTIVE INGREDIENT SECTION

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

Package Labeling:140ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

Package Labeling:70ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box2Box2

Package Labeling:50ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box3Box3

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79244-00179244-001-03, 79244-001-02, 79244-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYAMINOPROPYL BIGUANIDEDT9D8Z79ETIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ddce5f52-3c21-21f7-e053-2a95a90aa8641503ac37-493f-49cd-96fb-24dcb5a78d3f2022-04-29WarningsExact identifier
spl set id: 1503ac37-493f-49cd-96fb-24dcb5a78d3f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.