FDA.reportPublic FDA data

PROBLEND ANTIBACTERIAL CLEANSER

Manufacturer
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
Effective date
2019-12-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:46:57

Label at a glance#

ProductPROBLEND ANTIBACTERIAL CLEANSER
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

- Pump into hands, wet as needed. - Lather vigorously for at least 15 seconds. Wash skin, rinse thogoughly and dry. - Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

When Using this Product

GENERAL PRECAUTIONS SECTION

Avoid contact with eyes. In case of eye contact,, flush eyes with water.

Do not ingest. Stop use and contact a doctor if irritation or

redness develop or conditions persist for more than 72 hours. 

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help

or contact Poison Control Center right away.  

Directions

DOSAGE & ADMINISTRATION SECTION

- Pump into hands, wet as needed.

- Lather vigorously for at least 15 seconds. Wash skin, rinse thogoughly and dry.

- Children under 6 years of age should be supervised when using this product.

INERT INGREDIENTS:

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl Betaine, PEG 150 Distearate, Caprylyl Glucoside, Glycerine, Cocamide MIPA, Tetrasodium EDTA, Fragrance, Citric Acid, Aloe Vera, Benzisothiazol, Methylisothiozol, FD&C Blue #1

PROBLEND ANTIBACTERIAL LIQUID CLEANSER

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PROBLEND ANTIBACTERIAL LIQUID CLEANSERimage descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50241-98350241-983-01, 50241-983-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
CAPRYLYL GLUCOSIDEV109WUT6RLIACT
GLYCERINPDC6A3C0OXIACT
DITETRACYCLINE TETRASODIUM EDETATEWX0A0IT7K5IACT
BENZISOTHIAZOLINONEHRA0F1A4R3IACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT

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
43307448-c4b6-427f-8833-b1fcd612d2a537b0fa00-76c5-4130-b38a-aceab2be72832022-01-24WarningsExact identifier
spl set id: 37b0fa00-76c5-4130-b38a-aceab2be7283

Reported adverse events (FAERS/openFDA)#

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