ECOLAB Antiseptic

Manufacturer: Ecolab Food Safety Specialties, Inc. | Medique Products | Changzhou Maokang Medical Products Co., Ltd
Effective date: 2025-09-09
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-06-01 01:13:16

Label at a glance#

ProductECOLAB Antiseptic

Active ingredientBENZALKONIUM CHLORIDE

Label structure14 sections

Contacts and useful links#

PhoneLabel contact1-800-321-3687

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium Chloride, 0.133%

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

First aid to help reduce the risk of infection in minor cuts, scrapes and burns.

WARNINGS SECTION

Warnings

For external use only.

OTC - DO NOT USE SECTION

Do not use

in the eyes or over large areas of the body

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

deep punture wounds, animal bites or serious burns

OTC - STOP USE SECTION

Stop use and ask a doctor if

if the condition persists or gets worse

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.

DOSAGE & ADMINISTRATION SECTION

Directions

tear open packet, unfold and clean the affected area

OTHER SAFETY INFORMATION

Other information

store at room temperature 59°-86°F (15°-30°C)
tamper evident sealed packets
do not use any open or torn packets

INACTIVE INGREDIENT SECTION

Inactive ingredients

sodium bicarbonate, water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-321-3687

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANSI/ISEA Required

Ecolab® Antiseptic Wipes

Reorder # 22

Benzalonium chloride 0.133%

First Aid Antiseptic

20 extra large wipes per box

Tamper Evident Sealed Packets

ecolab

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1043307	benzalkonium chloride 1.33 MG/ML Medicated Pad	benzalkonium chloride 1.33 MG/ML Medicated Pad	SCD Active

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71338-225-71	ECOLAB Antiseptic	1.4 mL in 1 PACKET	LIQUID	1.4		7
71338-225-71	ECOLAB Antiseptic	20 in 1 BOX	LIQUID	20		7

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

ECOLAB Antiseptic
Benzalkonium Chloride
WATER
SODIUM BICARBONATE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71338-225	71338-225-71

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM BICARBONATE	8MDF5V39QO	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ECOLAB Antiseptic	BENZALKONIUM CHLORIDE	Ecolab Food Safety Specialties, Inc.	933860e7-5a1f-453a-e053-2995a90a4902	2025-09-09	Warnings	Exact identifier ndc (package): 71338-225-71 ndc (product): 71338-225 ndc11 (package): 71338022571 spl id: 3e5d8d37-6d85-4af8-e063-6394a90af668 spl set id: 933860e7-5a1f-453a-e053-2995a90a4902

Reported adverse events (FAERS/openFDA)#

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