FDA.reportPublic FDA data

MED NAP Benzalkonium Chloride Antiseptic

Manufacturer
Acme United Corporation
Effective date
2021-07-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:41:12

Label at a glance#

ProductMED NAP Benzalkonium Chloride Antiseptic
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Dosage and administration

•Tear at notch •Remove towelette •Use only once As a first aid antiseptic • Clean affected area •Apply 1 to 3 times daily •May be covered with a sterile bandage •If bandaged, let dry first

Storage and handling

•Store at room temperature •Avoid excessive heat

Label contents#

Full prescribing information#

Drug Facts Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Caution:

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.

Use:

INDICATIONS & USAGE SECTION

•First aid antisepticto help prevent skin infection in •Minor Cuts •Scrapes •Burns

•Antiseptic Cleansing •Perineal and maternity care.

Warnings

WARNINGS SECTION



For External Use Only.

Do not use •As an antiseptic for more than 1 week •in or around the eyes •Over large areas of the body.

Stop use

OTC - STOP USE SECTION

if irritation and redness develop •if condition persists more than 72 hours, consult a physician.

.

Directions

DOSAGE & ADMINISTRATION SECTION

•Tear at notch •Remove towelette •Use only once

As a first aid antiseptic •Clean affected area •Apply 1 to 3 times daily •May be covered with a sterile bandage •If bandaged, let dry first

Other Information

STORAGE AND HANDLING SECTION

•Store at room temperature •Avoid excessive heat

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, methylchloroisothiazolinone, methylisothiazolinone

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box Image

Box ImageBox Image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0924-0245-002025-02-01C16284748780-1f386c649-a772-0266-e053-dadaa90a7c1aMed Nap Benzalkonium Chloride Antiseptic Towelette
0924-0245-012025-02-01C16284748780-1f386c649-a772-0266-e053-dadaa90a7c1aMed Nap Benzalkonium Chloride Antiseptic Towelette
0924-0245-022025-02-01C16284748780-1f386c649-a772-0266-e053-dadaa90a7c1aMed Nap Benzalkonium Chloride Antiseptic Towelette
0924-0245-002023-01-30C16284748780-1f386c649-a772-0266-e053-dadaa90a7c1aMed Nap Benzalkonium Chloride Antiseptic Towelette
0924-0245-012023-01-30C16284748780-1f386c649-a772-0266-e053-dadaa90a7c1aMed Nap Benzalkonium Chloride Antiseptic Towelette
0924-0245-022023-01-30C16284748780-1f386c649-a772-0266-e053-dadaa90a7c1aMed Nap Benzalkonium Chloride Antiseptic Towelette

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0924-02450924-0245-00, 0924-0245-02, 0924-0245-01

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
NameUNIIKind
WATER059QF0KO0RIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
MAGNESIUM CHLORIDE ANHYDROUS59XN63C8VMIACT
MAGNESIUM NITRATE77CBG3UN78IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2d0511f4-a9f8-b373-e063-6394a90a8878c6b4850d-cbf0-048d-e053-2995a90ab22d2025-01-31WarningsExact identifier
spl set id: c6b4850d-cbf0-048d-e053-2995a90ab22d

Reported adverse events (FAERS/openFDA)#

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