FDA.reportPublic FDA data

Compliance Dishwashing Liquid and Antibacterial Hand

Manufacturer
Royal Paper Corp.
Effective date
2025-04-28
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 20:39:26

Label at a glance#

ProductCompliance Dishwashing Liquid and Antibacterial Hand
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 Handwashing

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 C14-16 Olefin Sulfonate (68439-57-6), Cocamidopropyl Hydroxysultaine (68139-30-), Benzenesulfonic Acid, C10-16-Alkyl Dervis. (68584-22-5), Sodium Chloride (7647-14-5), Propanediol (26264-14-2), Propylene Glycol (57-55-6), Sodium Hydroxide (1310-73-2), Sodium Polyitaconate (26099-89-8), Fragrance (Proprietary), 2-Bromo-2-Nitropropane-1,3-Diol (52-51-7), Methylisothiazolinone (2682-20-4), Methylchloroisothiazolinone (26172-55-4), Dibromocyanoacetamide (10222-01-2), Yellow 5 (1934-21-0), Red 40 (25956-17-6).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal displayPrincipal display

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59723-101COMPLIANCE DISHWASHING LIQUID AND ANTIBACTERIAL HAND (PCMX) SOAP [ROYAL PAPER CORP.]6Legacy NDC20250429_e5486dc8-d5a6-7aa6-e053-2a95a90a5248.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59723-10159723-101-41

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
SODIUM POLYITACONATE (2800 MW, PHOSPHATE TERMINATED)G7SW5QN7TTIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
PROPANEDIOL5965N8W85TIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
FD&C RED NO. 40WZB9127XOAIACT
SODIUM CHLORIDE451W47IQ8XIACT
EUGENOL3T8H1794QWIACT
WATER059QF0KO0RIACT
CINNAMALDEHYDESR60A3XG0FIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
CHLOROXYLENOL0F32U78V2QACTIB
DIBROMOCYANOACETAMIDE7N51QGL6MJIACT
BRONOPOL6PU1E16C9WIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT

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
33dc1c55-6d0c-e110-e063-6294a90ac0e5e5486dc8-d5a6-7aa6-e053-2a95a90a52482025-04-28WarningsExact identifier
spl id: 33dc1c55-6d0c-e110-e063-6294a90ac0e5
spl set id: e5486dc8-d5a6-7aa6-e053-2a95a90a5248

Reported adverse events (FAERS/openFDA)#

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