FDA.reportPublic FDA data

DEFENDER Antiseptic Foam Hand

Manufacturer
Scientific Molecular Technologies
Effective date
2021-06-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:40:42

Label at a glance#

ProductDEFENDER Antiseptic Foam Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand washing to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

Pump a small amount of foam into palm of hand. Run thoroughly over all surfaces of both hands for 15 seconds Rinse with potable water.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

  • For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

irritation or redness develops. If condition persists for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amount of foam into palm of hand.
  • Run thoroughly over all surfaces of both hands for 15 seconds
  • Rinse with potable water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, (aqua), butylene glycol,  Dihydroxypropyl PEG-5 linoleammonium chloride, Dihydroxyethyl cocamine oxide, glycereth-2 cocoate, Hydroxypropyl methylcellulose.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DE Fender  SCIENTIFIC MOLECULAR TECHNOLOGIES    ANTISEPTIC FOAM  Hand Soap    ELIMINATES 99.999% OF MOST COMMON GERMS THAT CAUSES ILLNESS   NO RINSE MOISTURIZES LEAVES SKIN SOFT  8.4 fl oz (250 ml)

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN4
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD4
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY4
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42953-000-002022-07-29C16284748780-1e4f33bdf-a777-d8a0-e053-dadaa90a6e4eDEFENDER Antiseptic Foam Hand
42953-000-012022-07-29C16284748780-1e4f33bdf-a777-d8a0-e053-dadaa90a6e4eDEFENDER Antiseptic Foam Hand

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42953-000-00DEFENDER Antiseptic Foam Hand250 mL in 1 BOTTLE, PUMPSOAP2504
42953-000-01DEFENDER Antiseptic Foam Hand1000 mL in 1 BOTTLE, PUMPSOAP10004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42953-000DEFENDER ANTISEPTIC FOAM HAND (BENZALKONIUM CHLORIDE) SOAP [SCIENTIFIC MOLECULAR TECHNOLOGIES]4Legacy NDC, 2 package rows20210603_d4eb0770-bc69-4801-9e2b-7d96d195f594.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W71
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y1
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA1
DIHYDROXYETHYL COCAMINE OXIDEINACTIVE INGREDIENT8AR51R3BL51
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDEINACTIVE INGREDIENT0Y0NQR2GH11
GLYCERETH-2 COCOATEINACTIVE INGREDIENTJWM00VS7HC1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
42953-00042953-000-00, 42953-000-01

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
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE0Y0NQR2GH1IACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
GLYCERETH-2 COCOATEJWM00VS7HCIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
c3cb9fff-d3fb-2c23-e053-2995a90aaa09d4eb0770-bc69-4801-9e2b-7d96d195f5942021-06-01WarningsExact identifier
spl id: c3cb9fff-d3fb-2c23-e053-2995a90aaa09
spl set id: d4eb0770-bc69-4801-9e2b-7d96d195f594

Reported adverse events (FAERS/openFDA)#

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