Simplify Antibacterial Hand

Manufacturer: Zhejiang Qimei Cosmetics Co., Ltd.
Effective date: 2023-12-12
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 21:18:31

Label at a glance#

ProductSimplify Antibacterial Hand Apple Blossom Scent

Active ingredientCHLOROXYLENOL

Label structure8 sections

Dosage and administration

Wet hands. Apply palmful to hands. Scrub thoroughly and rinse with water.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.30%

Purpose

OTC - PURPOSE SECTION

Antibacterial hand soap

Use

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

SPL UNCLASSIFIED SECTION

May cause moderate eye irritation. Avoid contact with eyes and skin. If in eyes, flush eyes gently with water for 15 minutes. If swallowed, drink water to dilute. If irritation persists, contact a Physician or Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands.
Apply palmful to hands.
Scrub thoroughly and rinse with water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Carbamide, citric acid, cocamidopropyl betaine, DMDM hydroton, dodecylbenzene sulfonic acid, ethyl alcohol, fragrance, lauramine oxide, sodium chloride, sodium hydroxide, sodium lauryl ether sulfate, sodium xylene sulfonate, water

19.4 FL OZ (1.21 PT) 573 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to

Dawn ^® Ultra Green Apple

Simplify _®

Antimicrobial

Hand Soap & Ultra Dish

Detergent

Contains no

phosphates

Cuts Grease

APPLE

BLOSSOM

SCENT

19.4 FL OZ (1.21 PT) 573 mL

FrontBack

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

Simplify Antibacterial Hand Apple Blossom Scent
Chloroxylenol
LAURAMINE OXIDE
SODIUM HYDROXIDE
SODIUM CHLORIDE
DODECYLBENZENESULFONIC ACID
WATER
UREA
SODIUM C12-14 ALKETH-3 SULFATE
ALCOHOL
COCAMIDOPROPYL BETAINE
SODIUM XYLENESULFONATE
ANHYDROUS CITRIC ACID
DMDM HYDANTOIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81773-013	81773-013-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LAURAMINE OXIDE	4F6FC4MI8W	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
CHLOROXYLENOL	0F32U78V2Q	ACTIB
DODECYLBENZENESULFONIC ACID	60NSK897G9	IACT
WATER	059QF0KO0R	IACT
UREA	8W8T17847W	IACT
SODIUM C12-14 ALKETH-3 SULFATE	5G80BO01PI	IACT
ALCOHOL	3K9958V90M	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
SODIUM XYLENESULFONATE	G4LZF950UR	IACT
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
29a65d9d-05ff-76dc-e063-6394a90ae36f			0287010b-405c-4c38-e063-6394a90a3314	2024-12-19	Warnings	Exact identifier spl set id: 0287010b-405c-4c38-e063-6394a90a3314

Reported adverse events (FAERS/openFDA)#

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