Antiseptic Wipes

Manufacturer: Front Line Safety
Effective date: 2025-12-15
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:23:05

Label at a glance#

ProductAntiseptic Wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Dosage and administration

• Clean the affected area. • May be covered with a sterile bandage. • If bandaged, let dry first.

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact1-888-900-2920

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

• First aid to prevent infection in minor cuts, scrapes, and burns.

Warnings

WARNINGS SECTION

For External Use Only

Do not use

OTC - DO NOT USE SECTION

• As an antiseptic for more than 1 week

• In the eyes

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

you have deep or puncture wounds, animal bites, or serious burns.

Stop use and ask a doctor if

OTC - STOP USE SECTION

• Irritation and redness develop

• Condition persists or get worse

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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Clean the affected area.

• May be covered with a sterile bandage.

• If bandaged, let dry first.

Other information

OTHER SAFETY INFORMATION

• Store at room temperature 15º-30ºC (59º-86°F).

• Avoid excessive heat.

•Tamper Evident. Do not use if packet is torn or cut.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

Questions?

OTC - QUESTIONS SECTION

1-888-900-2920 Monday-Friday, 8AM-4PM PST

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FL-2011_BX_MASTERFL-2011

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1038558	benzalkonium chloride 0.13 % Medicated Pad	PSN	3
1038558	benzalkonium chloride 1.3 MG/ML Medicated Pad	SCD	3
1038558	benzalkonium chloride 0.13 % Topical Cloth	SY	3
1038558	benzalkonium chloride 0.13 % Topical Swab	SY	3
1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Pad	SY	3
1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Swab	SY	3
1038558	benzalkonium chloride 1 ML per 750 ML Topical Swab	SY	3

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0814889010100	GTIN-13: 0814889010100 EAN-13: 0814889010100 GTIN-12: 814889010100 UPC-A: 814889010100 GTIN storage (14 digits): 00814889010100	FL-2011_BX_MASTER_R231106-3.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58228-6211-1	Antiseptic Wipes	20 in 1 BOX	SWAB	20		3
58228-6211-1	Antiseptic Wipes	480 in 1 CASE	SWAB	480		3

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Antiseptic Wipes
BENZALKONIUM CHLORIDE
BENZALKONIUM
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58228-6211	58228-6211-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	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
Antiseptic Wipes	ANTISEPTIC WIPES	Front Line Safety	0e1f3653-d75e-9c9e-e063-6294a90ab639	2025-12-15	Warnings	Exact identifier ndc (package): 58228-6211-1 ndc (product): 58228-6211 ndc11 (package): 58228621101 spl id: 46017cee-7ab8-f880-e063-6394a90a5a2e spl set id: 0e1f3653-d75e-9c9e-e063-6294a90ab639

Reported adverse events (FAERS/openFDA)#

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