FDA.reportPublic FDA data

Mosaic Lavender Hand

Manufacturer
Zhejiang iColor Biotech Co., Ltd
Effective date
2024-01-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:12:55

Label at a glance#

ProductMosaic Lavender Hand
Active ingredientCHLOROXYLENOL
Label structure7 sections

Indications and uses

For hand washing to decrease bacteria on skin.

Dosage and administration

Direction Wet hands. Apply small amount to hands. Scrub thoroughly. Rinse. For children under 6. use only under adult supervision.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

CHLOROXYLENOL 0.3%

Purpose

OTC - PURPOSE SECTION

Antimicrobical

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on skin.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Direction Wet hands. Apply small amount to hands. Scrub thoroughly. Rinse. For children under 6. use only under adult supervision.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Sodium Laureth Sulfate,Cocamide Methyl Mea,Cocamidopropyl Betaine,Glycerin,Sodium Citrate,Sodium Chloride,Tocopherol, Fragrance, Citric Acid, Alcohol,Methylisothiazolinone, Methylchloroisothiazolinone, Magnesium Chloride, Magnesium Nitrate,Disodium Edta.

Package Labeling:250ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74934-015MOSAIC LAVENDER HAND (CHLOROXYLENOL) LIQUID [ZHEJIANG ICOLOR BIOTECH CO., LTD]2Legacy NDC20240124_ce58af25-9cd9-482f-9451-671349ff397c.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74934-01574934-015-25, 74934-015-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURETH-3 SULFATEBPV390UAP0IACT
COCOYL METHYL MONOETHANOLAMINE79G1T427CFIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
GLYCERINPDC6A3C0OXIACT
SODIUM CITRATE1Q73Q2JULRIACT
SODIUM CHLORIDE451W47IQ8XIACT
TOCOPHEROLR0ZB2556P8IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ALCOHOL3K9958V90MIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
MAGNESIUM NITRATE77CBG3UN78IACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
CHLOROXYLENOL0F32U78V2QACTIB

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
0f9fff71-63f9-37eb-e063-6294a90a768ace58af25-9cd9-482f-9451-671349ff397c2024-01-23WarningsExact identifier
spl id: 0f9fff71-63f9-37eb-e063-6294a90a768a
spl set id: ce58af25-9cd9-482f-9451-671349ff397c

Reported adverse events (FAERS/openFDA)#

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