MEDISEPTIC ANTIINFECTANT

Manufacturer: PORTOFINO & ASSOCIATES, LLC
Effective date: 2022-05-09
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 22:01:42

Label at a glance#

ProductMEDISEPTIC ANTIINFECTANT

Active ingredientBENZALKONIUM CHLORIDE

Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.1% ..........ANTIBACTERIAL

OTC - PURPOSE SECTION

USE AS A HAND SANITISER TO HELP REDUCE BACTERIA ON SKIN
FOR HAND HYGIENE

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY. KEEP OUT OF REACH OF CHILDREN. NOT FOR FOOD USE. DO NOT INGEST.

OTC - WHEN USING SECTION

AVOID CONTACT WITH EYES. IN CASE OF EYE CONTACT, FLUSH EYES WITH WATER.

OTC - STOP USE SECTION

IF IRRITATION OR REDNESS DEVELOPS.

OTC - ASK DOCTOR SECTION

IF IRRITATION OR REDNESS PERSISTS MORE THAN 72 HOURS.

INSTRUCTIONS FOR USE SECTION

APPLY APPROX. 3-5MLS OF UNDILUTED PRODUCT INTO THE PALM OF HANDS AND RUB IN FOR 1 MINUTE. IN PARTICULAR TAKE INTO ACCOUNT THUMBS AND FINGERTIPS, AS THEY HAVE MOST FREQUENT CONTACT WITH CONTAMINATED SURFACES AND OBJECTS. FREQUENCY: REPEAT AS NEEDED TO RENEW PROTECTION.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

INACTIVE INGREDIENT SECTION

WATER, ORGANIC ACIDS, CATIONIC POLYMERS.

DOSAGE & ADMINISTRATION SECTION

READY TO USE. DO NOT DILUTE.

Other Information

OTHER SAFETY INFORMATION

Do not mix with acids and alkalis. Keep container tightly closed after use and keep cool.

Usage

INDICATIONS & USAGE SECTION

Use as a skin sanitizer to help reduce bacteria on skin. Repeat as necessary.

DRUG FACTS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ACTIVE INGREDIENTS PURPOSE

BENZALKONIUM CHLORIDE 0.1% .......ANTIBACTERIAL

LABEL $javascript:previewimage('May\u002026\u00202020\u0020MediSeptic_label_USA_50mL$ javascript:previewimage('May\u002026\u00202020\u0020MediSeptic_label_USA_50mL

Products#

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

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

MEDISEPTIC ANTIINFECTANT
BENZALKONIUM CHLORIDE
POVIDONE K15
BENZALKONIUM
WATER
GLYCERIN
CALCIUM FLUORIDE
SALICYLIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78874-500	78874-500-50, 78874-500-01, 78874-500-10, 78874-500-15, 78874-500-25, 78874-500-55, 78874-500-99, 78874-500-49, 78874-500-19, 78874-500-54, 78874-500-27, 78874-500-05, 78874-500-77

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POVIDONE K15	E54VE15114	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
CALCIUM FLUORIDE	O3B55K4YKI	IACT
SALICYLIC ACID	O414PZ4LPZ	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
de9dc309-bf16-7c97-e053-2a95a90a0d33			a76e69d3-e5df-2047-e053-2995a90ad942	2022-05-09	Warnings	Exact identifier spl id: de9dc309-bf16-7c97-e053-2a95a90a0d33 spl set id: a76e69d3-e5df-2047-e053-2995a90ad942

Reported adverse events (FAERS/openFDA)#

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