MOSAIC LAVENDER HAND- chloroxylenol liquid

Mosaic Lavender Hand by

Drug Labeling and Warnings

Mosaic Lavender Hand 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

CHLOROXYLENOL 0.3%

Purpose

Antimicrobical

Uses

For hand washing to decrease bacteria on skin.

Warnings

For external use only

When using this product

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

Keep out of reach of children.

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

Directions

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

Inactive ingredients

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 Labeling:500ml

INGREDIENTS AND APPEARANCE

MOSAIC LAVENDER HAND 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74934-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
TOCOPHEROL (UNII: R0ZB2556P8)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALCOHOL (UNII: 3K9958V90M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74934-015-25	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/08/2020	01/31/2026
2	NDC: 74934-015-50	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/08/2020	01/31/2026

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

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang iColor Biotech Co., Ltd		554528308	manufacture(74934-015)