FDA.reportPublic FDA data

HOBBY ANTIBACTERIAL HANDWASH

Manufacturer
Hobi Kozmetik Imalat Sanayi Ve Ticaret Anonim Sirketi
Effective date
2020-10-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:32:41

Label at a glance#

ProductHOBBY ANTIBACTERIAL HANDWASH
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Dosage and administration

Pump onto wet hands, vigorously work into a lather and rinse thoroughly.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% w/w

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

for washing hands to decrease bacteria on skin.

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with eyes, in case of eye contact, flush with water.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or go to Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Pump onto wet hands, vigorously work into a lather and rinse thoroughly.

Other information

OTHER SAFETY INFORMATION

Store in a cool dry place below 104 °F.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cocamidopropyl betaine, sodium laureth sulfate, cocamide DEA, lauryl glucoside, glycerin, fragrance, citric acid, benzophenone-4, propylene glycol, sodium chloride, benzyl alcohol, magnesium nitrate, methyIchloroisothiazolinone, methylisothiazolinone, red 33, blue 1

Principal Display Panel - 400 mL Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HOBBY®

Antibacterial
Liquid Hand Soap

BERRY MEDLEY

13.5 FL OZ
(400 ml)

Principal Display Panel - 400 mL Label
Principal Display Panel - 400 mL Label

Principal Display Panel - 400 mL Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HOBBY®

Antibacterial
Liquid Hand Soap

TROPICAL BEACH

13.5 FL OZ
(400 ml)

Principal Display Panel - 400 mL Label
Principal Display Panel - 400 mL Label

Principal Display Panel - 400 mL Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HOBBY®

Antibacterial
Liquid Hand Soap

PEACH DREAM

13.5 FL OZ
(400 ml)

Principal Display Panel - 400 mL Label
Principal Display Panel - 400 mL Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN2
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD2
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY2
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73789-0442-12025-01-30C16284748780-12cef2736-93a3-d83d-e063-dadaa90ab31fDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73789-0442-1HOBBY ANTIBACTERIAL HANDWASH6 in 1 CASELIQUID62
73789-0442-1HOBBY ANTIBACTERIAL HANDWASH400 mL in 1 BOTTLE, PUMPLIQUID4002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73789-0442HOBBY ANTIBACTERIAL HANDWASH (BENZALKONIUM CHLORIDE) LIQUID [HOBI KOZMETIK IMALAT SANAYI VE TICARET ANONIM SIRKETI]2Legacy NDC, 2 package rows20201031_eae72d60-b1fc-4bf1-b6b4-9d447e1a4fd2.zip

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73789-044273789-0442-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
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
LIMONENE, (+)-GFD7C86Q1WIACT
D&C RED NO. 339DBA0SBB0LIACT
GLYCERINPDC6A3C0OXIACT
SULISOBENZONE1W6L629B4KIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
BENZYL ALCOHOLLKG8494WBHIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
Magnesium CitrateRHO26O1T9VIACT
Propylene Glycol6DC9Q167V3IACT
LINALOOL, (+/-)-D81QY6I88EIACT
FD&C YELLOW NO. 6H77VEI93A8IACT
Benzyl BenzoateN863NB338GIACT
Benzyl SalicylateWAO5MNK9TUIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
Magnesium Nitrate77CBG3UN78IACT

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
86515173-a1d8-49fa-b8bf-6a99cd20bd4eeae72d60-b1fc-4bf1-b6b4-9d447e1a4fd22020-10-23WarningsExact identifier
spl id: 86515173-a1d8-49fa-b8bf-6a99cd20bd4e
spl set id: eae72d60-b1fc-4bf1-b6b4-9d447e1a4fd2

Reported adverse events (FAERS/openFDA)#

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