FDA.reportPublic FDA data

Altra Antimicrobial Foaming Hand Wash w/ Benzalkonium Chloride

Manufacturer
Buckeye International, Inc.
Effective date
2024-11-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:33:55

Label at a glance#

ProductAltra Antimicrobial Foaming Hand Wash w/ Benzalkonium Chloride
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Hand wash to help reduce bacteria on skin Recommended for repeated use

Dosage and administration

Wet hands and wrists Dispense an adequate amount of soap and vigorously wash hands Rinse hands thoroughly with clean or potable water Dry hands completely

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • Hand wash to help reduce bacteria on skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product do not use in or near eyes.

If in eyes, flush thoroughly with water.

OTC - STOP USE SECTION

If irritation or rash appears and persists, stop use and see a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, call a physician or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands and wrists
  • Dispense an adequate amount of soap and vigorously wash hands
  • Rinse hands thoroughly with clean or potable water
  • Dry hands completely

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Cetrimonium Chloride, Tetrasodium EDTA, Phenoxyethanol, Citric Acid.

Questions?

OTC - QUESTIONS SECTION

Call: Buckeye International, Inc. 314-291-1900

Monday through Friday 8:00 a.m. to 5:00 p.m. CST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Low Profile

ALTRA

Antimicrobial

Foaming

Hand Wash

w/ Benzalkonium Chloride

Hand Hygiene

NET CONTENTS 1000 mL (33.8 fl oz)

container labelcontainer label

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
30805-018-09Altra Antimicrobial Foaming Hand Wash w/ Benzalkonium Chloride1000 mL in 1 BAGSOLUTION10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30805-018ALTRA ANTIMICROBIAL FOAMING HAND WASH W/ BENZALKONIUM CHLORIDE (BENZALKONIUM CHLORIDE) SOLUTION [BUCKEYE INTERNATIONAL, INC.]1Current NDC, 1 package rows20241105_2618ecdc-3eeb-a69b-e063-6394a90a8024.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30805-01830805-018-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WATER059QF0KO0RIACT
TETRASODIUM EDTAMP1J8420LUIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT

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
Altra Antimicrobial Foaming Hand Wash w/ Benzalkonium ChlorideBENZALKONIUM CHLORIDEBuckeye International, Inc.2618ecdc-3eeb-a69b-e063-6394a90a80242024-11-04WarningsExact identifier
ndc (package): 30805-018-09
ndc (product): 30805-018
ndc11 (package): 30805001809
spl id: 2618ecdc-3eec-a69b-e063-6394a90a8024
spl set id: 2618ecdc-3eeb-a69b-e063-6394a90a8024

Reported adverse events (FAERS/openFDA)#

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