FDA.reportPublic FDA data

Dynarex Green

Manufacturer
Dynarex Corporation
Effective date
2024-11-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:38:20

Label at a glance#

ProductDynarex Green
Active ingredientCHLOROXYLENOL
Label structure9 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                         Purpose

Chloroxylenol 0.15%                   Antiseptic

WARNINGS

WARNINGS SECTION

  • For external use only
  • When using this product avoid contact with eyes. In case of contact, flush with water.

PURPOSE

OTC - PURPOSE SECTION

An antiseptic handwash.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop.

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Cleaning and antiseptic cleansing of hands and skin.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

  • Wet hands and forearms. Apply 5 milliliters (teaspoon) or palmful to hands and forearms. Scrub thoroughly for 1 minute. Rinse and repeat.

KEEP OUT OF REACH OF CHILDREN

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.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Inactive ingredients: Citric acid, Cocamidopropyl betaine, Cocmide DEA, D&C Red #33, Disodium EDTA, Frgarance, Glycerin, Sodium chloride, Sodium Lauryl Sulphate, Sodium o-phenylphenate, water.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dynarex Antibacterial Soap

1438 Soap.jpg

antibacterial soapantibacterial soap

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67777-318-01Dynarex Green221 mL in 1 BOTTLELIQUID2216

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67777-318DYNAREX GREEN (CHLOROXYLENOL) LIQUID [DYNAREX CORPORATION]6Current NDC, Legacy NDC, 1 package rows20241122_59b098d2-08de-4fdb-a209-ae226abf37d6.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67777-31867777-318-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
COCO DIETHANOLAMIDE92005F972DIACT
EDETATE DISODIUM7FLD91C86KIACT
GLYCERINPDC6A3C0OXIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM CHLORIDE451W47IQ8XIACT
WATER059QF0KO0RIACT
SODIUM O-PHENYLPHENATEKFV9K7N7UIIACT
D&C RED NO. 339DBA0SBB0LIACT
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
Dynarex GreenCHLOROXYLENOLDynarex Corporation59b098d2-08de-4fdb-a209-ae226abf37d62024-11-20WarningsExact identifier
ndc (package): 67777-318-01
ndc (product): 67777-318
ndc11 (package): 67777031801
spl id: 27592928-80cb-ccea-e063-6394a90abf6b
spl set id: 59b098d2-08de-4fdb-a209-ae226abf37d6

Reported adverse events (FAERS/openFDA)#

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