DEFENSE Hand Sanitizer Spray

Manufacturer
Walla Walla Environmental, Inc.
Effective date
2022-08-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:50:35

Label at a glance#

ProductDEFENSE Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

Dosage and administration

• Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age.
  • on open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

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

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

SPL UNCLASSIFIED SECTION

  • Store between 15-30C (50-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, lemongrass essential oil, glycerin, hydrogen peroxide

Package Labeling:60ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

Package Labeling:236.5ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box2Box2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039900isopropyl alcohol 75 % Topical SolutionPSN3
1039900isopropyl alcohol 0.75 ML/ML Topical SolutionSCD3
1039900isopropyl alcohol 75 % Topical SolutionSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80579-000-01DEFENSE Hand Sanitizer60 mL in 1 BOTTLELIQUID603
80579-000-02DEFENSE Hand Sanitizer236.588 mL in 1 BOTTLELIQUID236.5883

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80579-000DEFENSE HAND SANITIZER (ISOPROPYL ALCOHOL) LIQUID [WALLA WALLA ENVIRONMENTAL, INC.]3Current NDC, Legacy NDC, 2 package rows20220901_af49488d-5aeb-e3d9-e053-2a95a90afb04.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80579-00080579-000-01, 80579-000-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
DEFENSE Hand SanitizerISOPROPYL ALCOHOLWalla Walla Environmental, Inc.af49488d-5aeb-e3d9-e053-2a95a90afb042022-08-31WarningsExact identifier
ndc (package): 80579-000-01
ndc (package): 80579-000-02
ndc (product): 80579-000
ndc11 (package): 80579000001
ndc11 (package): 80579000002
spl id: e78c56df-0644-644c-e053-2a95a90a5388
spl set id: af49488d-5aeb-e3d9-e053-2a95a90afb04

Reported adverse events (FAERS/openFDA)#

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