FDA.reportPublic FDA data

Bortek E-2 Foaming Hand Wash

Manufacturer
Bortek Industries
Effective date
2023-01-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:39:23

Label at a glance#

ProductBortek E-2 Foaming Hand Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium chloride 0.13% w/w

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

Handwash to decrease bacteria on the skin that can potentially cause disease.

WARNINGS SECTION

Warnings

For external use only.

OTC - WHEN USING SECTION

When using this product keep away from eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Pump suffIcient amount of foam into palm of hand
  • Rub foam thoroughly over all surfaces of both hands for 15 seconds, including the area under the fingernails
  • Rinse with water and dry thoroughly.

INACTIVE INGREDIENT SECTION

Inactive ingredients

alcohol, cetrimonium chloride, chlorhexidine gluconate, cocamidopropyl PG-dimonium chloride phosphate, decyl glucoside, isopropyl alcohol, phenoxyethanol, polyquatemium 10, polyquatemium 11, water.

SPL UNCLASSIFIED SECTION

800-626-7835

BortekShop.com

Distributed by Bortek Industries, Inc., Mechanicsburg, PA 17055

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bortek® INDUSTRIES, INC.

E-2 ANTISEPTIC FOAMING HAND WASH

33.8 fl oz (1000 mL)

3- E-2 HS 81731-401 FINAL3- E-2 HS 81731-401 FINAL

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81731-40181731-401-01, 81731-401-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
CHLORHEXIDINE GLUCONATEMOR84MUD8EIACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
DECYL GLUCOSIDEZ17H97EA6YIACT
ALCOHOL3K9958V90MIACT
ISOPROPYL ALCOHOLND2M416302IACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
POLYQUATERNIUM-11 (1000000 MW)0B44BS5IJSIACT
WATER059QF0KO0RIACT
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
f278ffa7-5098-06fc-e053-2995a90a6bb9bfcd86f2-17b2-a5a8-e053-2995a90ac1dd2023-01-17WarningsExact identifier
spl id: f278ffa7-5098-06fc-e053-2995a90a6bb9
spl set id: bfcd86f2-17b2-a5a8-e053-2995a90ac1dd

Reported adverse events (FAERS/openFDA)#

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