Durisan

Manufacturer: Sanit Technologies LLC | Durisan
Effective date: 2020-12-02
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 23:34:29

Label at a glance#

ProductDurisan

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Dosage and administration

Pump onto dry skin. Lather vigorously for 20 seconds. Rinse hands and dry thoroughly.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of contact eyes with water.

Stop use and consult a doctor if irritation or redness develops.

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

Pump onto dry skin. Lather vigorously for 20 seconds.
Rinse hands and dry thoroughly.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, cocamidopropyl betaine, glycerin, cetrimonium chloride, benzyl alcohol, disodium EDTA, benzoic acid, sorbic acid

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1233282	benzalkonium chloride 0.1 % Medicated Liquid Soap	PSN	4
1233282	benzalkonium chloride 1 MG/ML Medicated Liquid Soap	SCD	4
1233282	benzalkonium chloride 0.1 % Medicated Liquid Soap	SY	4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71120-117-01	2021-07-23	C162847	48780-1	c7ccaba7-18ff-fd44-e053-dadaa90aa01b	4639cf1b-198b-400d-81bb-8640a593cff7
71120-117-02	2021-07-23	C162847	48780-1	c7ccaba7-18ff-fd44-e053-dadaa90aa01b	4639cf1b-198b-400d-81bb-8640a593cff7
71120-117-03	2021-07-23	C162847	48780-1	c7ccaba7-18ff-fd44-e053-dadaa90aa01b	4639cf1b-198b-400d-81bb-8640a593cff7
71120-117-04	2021-07-23	C162847	48780-1	c7ccaba7-18ff-fd44-e053-dadaa90aa01b	4639cf1b-198b-400d-81bb-8640a593cff7
71120-117-05	2021-07-23	C162847	48780-1	c7ccaba7-18ff-fd44-e053-dadaa90aa01b	4639cf1b-198b-400d-81bb-8640a593cff7
71120-117-06	2021-07-23	C162847	48780-1	c7ccaba7-18ff-fd44-e053-dadaa90aa01b	4639cf1b-198b-400d-81bb-8640a593cff7
71120-117-07	2021-07-23	C162847	48780-1	c7ccaba7-18ff-fd44-e053-dadaa90aa01b	4639cf1b-198b-400d-81bb-8640a593cff7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
71120-117-01	Durisan	300 mL in 1 PACKAGE	LIQUID	300	4
71120-117-02	Durisan	1000 mL in 1 PACKAGE	LIQUID	1000	4
71120-117-03	Durisan	3785 mL in 1 PACKAGE	LIQUID	3785	4
71120-117-04	Durisan	50 mL in 1 PACKAGE	LIQUID	50	4
71120-117-05	Durisan	550 mL in 1 PACKAGE	LIQUID	550	4
71120-117-06	Durisan	250 mL in 1 PACKAGE	LIQUID	250	4
71120-117-07	Durisan	1000 mL in 1 PACKAGE	LIQUID	1000	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71120-117	DURISAN (BENZALKONIUM CHLORIDE) LIQUID [SANIT TECHNOLOGIES LLC]	4	Legacy NDC, 7 package rows	20201203_4639cf1b-198b-400d-81bb-8640a593cff7.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

Durisan
BENZALKONIUM CHLORIDE
BENZALKONIUM
WATER
COCAMIDOPROPYL BETAINE
GLYCERIN
CETRIMONIUM CHLORIDE
BENZYL ALCOHOL
EDETATE DISODIUM ANHYDROUS
BENZOIC ACID
SORBIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71120-117	71120-117-01, 71120-117-02, 71120-117-03, 71120-117-04, 71120-117-05, 71120-117-06, 71120-117-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
GLYCERIN	PDC6A3C0OX	IACT
CETRIMONIUM CHLORIDE	UC9PE95IBP	IACT
BENZYL ALCOHOL	LKG8494WBH	IACT
EDETATE DISODIUM ANHYDROUS	8NLQ36F6MM	IACT
BENZOIC ACID	8SKN0B0MIM	IACT
SORBIC ACID	X045WJ989B	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f8f9c2a2-35df-4ff8-8d00-a7d285260797			4639cf1b-198b-400d-81bb-8640a593cff7	2020-12-02	Warnings	Exact identifier spl id: f8f9c2a2-35df-4ff8-8d00-a7d285260797 spl set id: 4639cf1b-198b-400d-81bb-8640a593cff7

Reported adverse events (FAERS/openFDA)#

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