ProCure Foaming Antimicrobial Hand

Manufacturer
Twin Med LLC
Effective date
2025-09-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:12:40

Label at a glance#

ProductProCure Foaming Antimicrobial Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Uses handwashing to help decrease bacteria on the skin

Dosage and administration

Directions wet hands apply product and thoroughly cover hands with lather for 30 seconds rinse well and dry hands completely

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Uses handwashing to help decrease bacteria on the skin

Warnings

WARNINGS SECTION

Warnings

For external use only

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and lasts more than 72 hours

Keep out of reach of children.

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

Directions

  • wet hands
  • apply product and thoroughly cover hands with lather for 30 seconds
  • rinse well and dry hands completely

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Laurtrimonium Chloride, Cocamidopropyl Betaine, PEG-6 Cocamide, Cocamidopropyl PG-Dimonium Chloride Phosphate, Fragrance, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Methylisothiazolinone, Iodopropynyl Butylcarbamate, Yellow # 5, Red # 33

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Foaming Hand Soap ImageFoaming Hand Soap Image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN1
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD1
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY1
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55681-042-10ProCure Foaming Antimicrobial Hand1000 mL in 1 CARTRIDGESOAP10001

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
55681-04255681-042-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
ProCure Foaming Antimicrobial HandHAND SOAP (BENZALKONIUM CHLORIDE 0.13%)Twin Med LLC3e002cee-6102-1db4-e063-6394a90ac7a12025-09-04WarningsExact identifier
ndc (package): 55681-042-10
ndc (product): 55681-042
ndc11 (package): 55681004210
spl id: 3e002cee-6103-1db4-e063-6394a90ac7a1
spl set id: 3e002cee-6102-1db4-e063-6394a90ac7a1

Reported adverse events (FAERS/openFDA)#

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