FOAMING HAND

Manufacturer
Draco Hygienic Products Inc.
Effective date
2024-10-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:23:11

Label at a glance#

ProductFOAMING HAND ANTIBACTERIAL
Active ingredientCHLOROXYLENOL
Label structure9 sections

Dosage and administration

WET HANDS AND FOREARMS. APPLY A SMALL AMOUNT OF SOAP AND SCRUB THOROUGHLY FOR 1 MINUTE. RINSE THOROUGHLY. DRY HANDS COMPLETELY.

Storage and handling

Store below 20-25°C (60 TO 77°F)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

CHLOROXYLENOL @ 0.45%

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USE

INDICATIONS & USAGE SECTION

HELP PREVENT CROSS CONTAMINATION BY HAND CONTACT TO REDUCE INCIDENCE ON NOSOCOMIAL INFECTION.

WARNINGS

WARNINGS SECTION

For external use only.

WHEN USING THIS PRODUCT

  • AVOID CONTACT WITH EYES. IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER.
  • AVOID CONTACT WITH BROKEN SKIN.

STOP USE THIS PRODUCT AND ASK A DOCTOR IF

  • CONDITIONS WORSEN OR IRRITATION PERSISTS.
  • IRRITATION OR REDNESS DEVELOPS AND PERSISTED FOR MORE THAN 72 HOURS.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children
lf swallowed,get medical help or contact Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • WET HANDS AND FOREARMS.
  • APPLY A SMALL AMOUNT OF SOAP AND SCRUB THOROUGHLY FOR 1 MINUTE.
  • RINSE THOROUGHLY.
  • DRY HANDS COMPLETELY.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

  • Store below 20-25°C (60 TO 77°F)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Propylene Glycol, Polyquaternium 7, Fragrance, Citric Acid, Color Dye.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

lbllbl

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2002728chloroxylenol 0.45 % Medicated Liquid SoapPSN2
2002728chloroxylenol 4.5 MG/ML Medicated Liquid SoapSCD2
2002728chloroxylenol 0.45 % Medicated Liquid SoapSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83019-103-11FOAMING HANDANTIBACTERIAL1000 mL in 1 CONTAINERSOAP10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83019-103FOAMING HAND ANTIBACTERIAL (CHLOROXYLENOL) SOAP [DRACO HYGIENIC PRODUCTS INC.]2Current NDC, 1 package rows20241010_15256355-29ef-9b24-e063-6294a90a907d.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83019-10383019-103-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
FOAMING HAND ANTIBACTERIALCHLOROXYLENOLDraco Hygienic Products Inc.15256355-29ef-9b24-e063-6294a90a907d2024-10-08WarningsExact identifier
ndc (package): 83019-103-11
ndc (product): 83019-103
ndc11 (package): 83019010311
spl id: 23f9338f-4538-64ed-e063-6394a90ada99
spl set id: 15256355-29ef-9b24-e063-6294a90a907d

Reported adverse events (FAERS/openFDA)#

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