DSC Antibacterial

Manufacturer: Crystalline Heath & Beauty From The DEad Sea LTD
Effective date: 2022-06-01
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 22:00:16

Label at a glance#

ProductDSC Antibacterial

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Dosage and administration

Use whenever washing your hands. Rinse with warm water.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Help eliminate bacteria on hands.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes, ears and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness persists.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Use whenever washing your hands. Rinse with warm water.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water/Aqua, Sodium Laureth Sulphate, Sodium Chloride, Cocamidopropyl Betaine, Glycerin, Maris Sal (Dead Sea Minerals), Fragrance (Parfum),Citrus Medica Limonum (Lemon) Peel Extract, Chamomilla Recutita Flower Extract,DMDM Hydantoin, Triethylene Glycol, Propylene Glycol, Benzyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone, Magnesium Nitrate, Magnesium Chloride,Tetrasodium EDTA, Citric Acid.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

DSC Antibacterial
BENZALKONIUM CHLORIDE
WATER
SODIUM CHLORIDE
COCAMIDOPROPYL BETAINE
GLYCERIN
LEMON PEEL
CHAMOMILE
DMDM HYDANTOIN
TRIETHYLENE GLYCOL
PROPYLENE GLYCOL
BENZYL ALCOHOL
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
MAGNESIUM NITRATE
MAGNESIUM CHLORIDE
EDETATE SODIUM
CITRIC ACID MONOHYDRATE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71095-012	71095-012-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
GLYCERIN	PDC6A3C0OX	IACT
LEMON PEEL	72O054U628	IACT
CHAMOMILE	FGL3685T2X	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
TRIETHYLENE GLYCOL	3P5SU53360	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
BENZYL ALCOHOL	LKG8494WBH	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
MAGNESIUM NITRATE	77CBG3UN78	IACT
MAGNESIUM CHLORIDE	02F3473H9O	IACT
EDETATE SODIUM	MP1J8420LU	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
e0697070-c52b-62e2-e053-2995a90a07b6			a825166c-fabf-06b1-e053-2995a90a58cf	2022-06-01	Warnings	Exact identifier spl id: e0697070-c52b-62e2-e053-2995a90a07b6 spl set id: a825166c-fabf-06b1-e053-2995a90a58cf

Reported adverse events (FAERS/openFDA)#

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