FDA.reportPublic FDA data

BRIGHTON PROFESSIONAL Antibacterial Plum Foam Handwash

Manufacturer
Staples
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:47:36

Label at a glance#

ProductBRIGHTON PROFESSIONAL Antibacterial Plum Foam Handwash
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

• Handwash to help decrease bacteria on the skin • Recommended for repeated use

Dosage and administration

• Wet hands • Apply a small amount of product and work into a lather • Rinse well and dry hands completely

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.5%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

• Handwash to help decrease bacteria on the skin

• Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor ifirritation or rash appears and lasts

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.

Directions

DOSAGE & ADMINISTRATION SECTION

• Wet hands

• Apply a small amount of product and work into a lather

• Rinse well and dry hands completely

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Propylene Glycol, Glycerin, Cocamidopropyl Betaine, PEG-80 Sorbitan Laurate, Citric Acid, Ethylhexylglycerin, Lauramine Oxide, Polyquaternium-10, Fragrance (Parfum), Phenoxyethanol, Blue 1 (CI 42090), Red 33 (CI 17200)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49514-400-23BRIGHTON PROFESSIONAL Antibacterial Plum Foam Handwash700 mL in 1 PACKAGELIQUID7003
49514-400-40BRIGHTON PROFESSIONAL Antibacterial Plum Foam Handwash1200 mL in 1 PACKAGELIQUID12003
49514-400-42BRIGHTON PROFESSIONAL Antibacterial Plum Foam Handwash1250 mL in 1 PACKAGELIQUID12503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49514-400BRIGHTON PROFESSIONAL ANTIBACTERIAL PLUM FOAM HANDWASH (BENZALKONIUM CHLORIDE) LIQUID [STAPLES]3Current NDC, Legacy NDC, 3 package rows20241222_845f4281-408c-47b4-bbf0-4f248deadc35.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49514-40049514-400-23, 49514-400-40, 49514-400-42

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PEG-80 SORBITAN LAURATE239B50Y732IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
POLYQUATERNIUM-10 (10000 MPA.S AT 2%)PI1STR9QYHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT
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
BRIGHTON PROFESSIONAL Antibacterial Plum Foam HandwashBENZALKONIUM CHLORIDEStaples845f4281-408c-47b4-bbf0-4f248deadc352024-12-19WarningsExact identifier
ndc (package): 49514-400-40
ndc (package): 49514-400-23
ndc (package): 49514-400-42
ndc (product): 49514-400
ndc11 (package): 49514040040
ndc11 (package): 49514040042
ndc11 (package): 49514040023
spl id: 29a2c3fb-f305-14fc-e063-6394a90ab26e
spl set id: 845f4281-408c-47b4-bbf0-4f248deadc35

Reported adverse events (FAERS/openFDA)#

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