PRIME SOURCE SELECT Plum Antibacterial Foam Hand So ap

Manufacturer
BUNZL
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:47:56

Label at a glance#

ProductPRIME SOURCE SELECT Plum Antibacterial Foam Hand So ap
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
66294-402-40PRIME SOURCE SELECT Plum Antibacterial Foam Hand So ap1200 mL in 1 PACKAGELIQUID12003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66294-402PRIME SOURCE SELECT PLUM ANTIBACTERIAL FOAM HAND SO AP (BENZALKONIUM CHLORIDE) LIQUID [BUNZL]3Current NDC, Legacy NDC, 1 package rows20241222_d56dbf55-9630-4d00-9dc5-68e55f48e793.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
66294-40266294-402-40

Ingredients#

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

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

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
PRIME SOURCE SELECT Plum Antibacterial Foam Hand So apBENZALKONIUM CHLORIDEBUNZLd56dbf55-9630-4d00-9dc5-68e55f48e7932024-12-19WarningsExact identifier
ndc (package): 66294-402-40
ndc (product): 66294-402
ndc11 (package): 66294040240
spl id: 29a0de93-f4df-335e-e063-6394a90a1aee
spl set id: d56dbf55-9630-4d00-9dc5-68e55f48e793

Reported adverse events (FAERS/openFDA)#

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