FDA.reportPublic FDA data

Max OUT

Manufacturer
Unico | Dan-Mor
Effective date
2026-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:31:02

Label at a glance#

ProductMax OUT
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

Wipex MAX OUT! Value Sanitizing Wipes Refill Bag

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Contrl right away.

Warnings

WARNINGS SECTION

For external use only. Avoid cntact with the eyes. If in eyes, flush thoroughly with water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium benzoate, sodium chloride, citric acid, potassium sorbate, sodium hydroxymethylglycinate, aloe vera leaf, water

Purpose

OTC - PURPOSE SECTION

Antiseptic

Stop Use

OTC - STOP USE SECTION

Stop and ask a doctor if:


Irritation or redness developes.


Conditions persists for more than 72 hours.

To Use

DOSAGE & ADMINISTRATION SECTION

Sanitize hands or other affected area. Discard in trash after use.

To dispense

INDICATIONS & USAGE SECTION

To begin: Break tab on bucket rim and pull off cover. Open bag inside to expose wipes, then thread center wipe through the lid. Replace bucket cover to maintain moisture.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Max OUTMax OUT

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74680-221-88Max OUT480 mL in 1 CANCLOTH4801

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74680-22174680-221-88

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM CHLORIDE451W47IQ8XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM HYDROXYMETHYLGLYCINATEDIG6BWZ9XTIACT
SODIUM BENZOATEOJ245FE5EUIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT

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
Max OUTBENZALKONIUM CHLORIDEUnico475903d2-a0b0-5d29-e063-6394a90a528f2026-01-01WarningsExact identifier
ndc (package): 74680-221-88
ndc (product): 74680-221
ndc11 (package): 74680022188
spl id: 475903d2-a0b1-5d29-e063-6394a90a528f
spl set id: 475903d2-a0b0-5d29-e063-6394a90a528f

Reported adverse events (FAERS/openFDA)#

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