FDA.reportPublic FDA data

ANTIBACTERIAL HANDWASH

Manufacturer
Hobi Kozmetik Imalat Sanayi Ve Ticaret Anonim Sirketi
Effective date
2020-03-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:38:09

Label at a glance#

ProductANTIBACTERIAL HANDWASH HOBBY
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

Handwash to help decrease bacteria on skin Recommended for repeated use

Dosage and administration

wet hands apply a small amount of product and work into lather rinse well and dry hands completely

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

  • Handwash to help decrease bacteria on skin
  • Recommended for repeated use

WARNING

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

  • do not use in or near eyes
  • In case of eye contact, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation occurs or rash appears and last

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • wet hands
  • apply a small amount of product and work into lather
  • rinse well and dry hands completely

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water（Aqua),Sodium Laureth Sulfate,Cocamidopropyl Betaine,Coconut Monoethanol Amide,Sodium Chloride,Fragrance,Citric Acid,Methylchloroisothiazolinone,Methylisothiazolinone,D&C Red No.33,FD&C Blue No.1, FD&C Red No. 40, FD&C Yellow No. 5

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug fact panel 2Drug fact panel 2Drug Fact PanelDrug Fact Panel

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73789-044073789-0440-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM CHLORIDE451W47IQ8XIACT
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
COCO DIETHANOLAMIDE92005F972DIACT
FD&C RED NO. 40WZB9127XOAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
LIMONENE, (+)-GFD7C86Q1WIACT
D&C RED NO. 339DBA0SBB0LIACT
GLYCERINPDC6A3C0OXIACT
SULISOBENZONE1W6L629B4KIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
BENZYL ALCOHOLLKG8494WBHIACT

Source Document#

Source XML · Source PDF

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
a2034c5c-0b2c-2980-e053-2995a90a75cca2034c5c-0b2b-2980-e053-2995a90a75cc2020-03-29WarningsExact identifier
spl id: a2034c5c-0b2c-2980-e053-2995a90a75cc
spl set id: a2034c5c-0b2b-2980-e053-2995a90a75cc

Reported adverse events (FAERS/openFDA)#

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