FDA.reportPublic FDA data

DEFENDER Antiseptic Foam Hand Sanitizer Alcohol-Free

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 Sanitizer Alcohol-Free
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

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

Dosage and administration

Pump a small amount of foam into palm of hand. Wet hands thoroughly with product and allow to dry without wiping. Rub hands together briskly until dry.

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 sanitizing to decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

  • For external use only.

Do not use in eyes

OTC - DO NOT USE SECTION

if contact occurs, flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

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.
  • Wet hands thoroughly with product and allow to dry without wiping.
  • Rub hands together briskly until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DE Fender  SCIENTIFIC MOLECULAR TECHNOLOGIES    ANTISEPTIC FOAM  Hand Sanitizer  ALCOHOL-FREE    ELIMINATES 99.999% OF MOST COMMON GERMS THAT CAUSES ILLNESS   NO RINSE MOISTURIZES LEAVES SKIN SOFT   EFFECTIVE AGAINST STAPH, MRSA, VRE, NOROVIRUS   1.7 fl oz (50 ml)

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN4
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD4
1020365benzalkonium chloride 0.13 % Topical FoamSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42953-002-002022-07-29C16284748780-1e4f33bdf-a7f9-d8a0-e053-dadaa90a6e4eDEFENDER Antiseptic Foam Hand Sanitizer Alcohol-Free
42953-002-012022-07-29C16284748780-1e4f33bdf-a7f9-d8a0-e053-dadaa90a6e4eDEFENDER Antiseptic Foam Hand Sanitizer Alcohol-Free
42953-002-022022-07-29C16284748780-1e4f33bdf-a7f9-d8a0-e053-dadaa90a6e4eDEFENDER Antiseptic Foam Hand Sanitizer Alcohol-Free

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42953-002-00DEFENDER Antiseptic Foam Hand Sanitizer Alcohol-Free50 mL in 1 BOTTLE, PUMPLIQUID504
42953-002-01DEFENDER Antiseptic Foam Hand Sanitizer Alcohol-Free550 mL in 1 BOTTLE, PUMPLIQUID5504
42953-002-02DEFENDER Antiseptic Foam Hand Sanitizer Alcohol-Free1000 mL in 1 BOTTLE, PUMPLIQUID10004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42953-002DEFENDER ANTISEPTIC FOAM HAND SANITIZER ALCOHOL-FREE (BENZALKONIUM CHLORIDE) LIQUID [SCIENTIFIC MOLECULAR TECHNOLOGIES]4Legacy NDC, 3 package rows20210603_fd6a24a0-a0c7-41cc-b5db-d2d232d1b636.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W71
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y1
BEHENTRIMONIUM CHLORIDEINACTIVE INGREDIENTX7GNG3S47T1
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
42953-00242953-002-00, 42953-002-01, 42953-002-02

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
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE0Y0NQR2GH1IACT
GLYCERETH-2 COCOATEJWM00VS7HCIACT
BEHENTRIMONIUM CHLORIDEX7GNG3S47TIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
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
c3ca16f9-0e5d-06c9-e053-2995a90a0daafd6a24a0-a0c7-41cc-b5db-d2d232d1b6362021-06-01WarningsExact identifier
spl id: c3ca16f9-0e5d-06c9-e053-2995a90a0daa
spl set id: fd6a24a0-a0c7-41cc-b5db-d2d232d1b636

Reported adverse events (FAERS/openFDA)#

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