Antibacterial White Pearl

Manufacturer: Morrisette Paper Company, Inc.
Effective date: 2025-07-14
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: full-release
Hydrated at: 2026-06-01 01:07:56

Label at a glance#

ProductAntibacterial White Pearl

Active ingredientCHLOROXYLENOL

Label structure9 sections

Indications and uses

• Handwash to help decrease bacteria on the skin.

Dosage and administration

• Apply a small amount of product to wet hands, work into lather for 30 seconds, and rinse thoroughly. • Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• Handwash to help decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.
Do not use in the eyes. In case of contact, immediately flush eyes with water.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control
Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply a small amount of product to wet hands, work into lather for 30 seconds, and rinse thoroughly.
• Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua) (7732-18-5), Sodium Lauryl Sulfate (68585-47-7), Cocamidopropyl Hydroxysultaine (68139-30-0), Sodium Chloride (7647-14-5), Propanediol (26264-14-2), Propylene Glycol (57-55-6), Sodium C14-16 Olefin Sulfonate (68439-57-6), Glycol Distearate (627-83-8), Fragrance (Proprietary), Sodium Citrate (6132-04-3), Methylisothiazolinone (2682-20-4), Methylchloroisothiazolinone (26172-55-4), 2-Bromo-2- Nitropropane-1,3-Diol (52-51-7).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1941461	chloroxylenol 0.1 % Medicated Liquid Soap	PSN	6
1941461	chloroxylenol 1 MG/ML Medicated Liquid Soap	SCD	6
1941461	chloroxylenol 0.1 % Medicated Liquid Soap	SY	6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
82078-301-41	Antibacterial White Pearl	3.78 L in 1 BOTTLE, PLASTIC	SOAP	3.78		6

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

Antibacterial White Pearl
PCMX
SODIUM LAURYL SULFATE
SODIUM CHLORIDE
GLYCOL DISTEARATE
COCAMIDOPROPYL HYDROXYSULTAINE
PROPANEDIOL
PROPYLENE GLYCOL
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
WATER
SODIUM C14-16 OLEFIN SULFONATE
CHLOROXYLENOL
BRONOPOL
SODIUM CITRATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
82078-301	82078-301-41

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
SODIUM LAURYL SULFATE	368GB5141J	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
GLYCOL DISTEARATE	13W7MDN21W	IACT
COCAMIDOPROPYL HYDROXYSULTAINE	62V75NI93W	IACT
PROPANEDIOL	5965N8W85T	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
WATER	059QF0KO0R	IACT
SODIUM C14-16 OLEFIN SULFONATE	O9W3D3YF5U	IACT
CHLOROXYLENOL	0F32U78V2Q	ACTIB
BRONOPOL	6PU1E16C9W	IACT
SODIUM CITRATE	1Q73Q2JULR	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
Antibacterial White Pearl	PCMX	Morrisette Paper Company, Inc.	c976dad3-4ad3-be00-e053-2a95a90a73cd	2025-07-14	Warnings	Exact identifier ndc (package): 82078-301-41 ndc (product): 82078-301 ndc11 (package): 82078030141 spl id: 39e66059-42f2-19d7-e063-6294a90ac83f spl set id: c976dad3-4ad3-be00-e053-2a95a90a73cd

Reported adverse events (FAERS/openFDA)#

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