Defense Zone Sanitizer Spray

Manufacturer
Prime Packaging | Prime Enterprises
Effective date
2020-08-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:15

Label at a glance#

ProductDefense Zone Hand Sanitizer
Active ingredientALCOHOL
Label structure14 sections

Indications and uses

to decrease bacteria on the skin that could cause disease. recommrnded for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping. for children under 6, use only under adult supervision. not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease. recommrnded for repeated use

Warning

WARNINGS SECTION

For external use only

Dot not use

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

Keep away from face to avoid breathing it. Keep out of eyes. rinse with water to remove.

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

If irritation and redness occurs if condition persistes for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Posion Control Center right away.

Flammable

OTHER SAFETY INFORMATION

Avoid fire, flame, heat and smoking. Contents under pressre. do not punture or incinerate. Store at temperatures below 120°F(50°C).

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping. for children under 6, use only under adult supervision. not recommended for infants.

Other Information

OTHER SAFETY INFORMATION

do not store above 104°F. may discolor some fabrics. harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice,Glycerin,Isopropyl Myristate, Tocopherol,Water.

Questions

OTC - QUESTIONS SECTION

Call 1 855-548-4653

Principal display label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principle Display LabelPrinciple Display Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN1
1041849ethanol 0.7 ML/ML Topical SpraySCD1
1041849ethanol 70 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
13630-0161-42024-01-30C16284748780-11030e365-0550-111a-e063-dadaa90a10e2Defense Zone Sanitizer Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13630-0161-4Defense ZoneHand Sanitizer177 mL in 1 CANSPRAY1771

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13630-0161DEFENSE ZONE HAND SANITIZER (ETHYL ALCOHOL) SPRAY [PRIME PACKAGING]1Legacy NDC, 1 package rows20201009_ad152870-0168-d1e7-e053-2995a90ad3ed.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
13630-016113630-0161-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
ad152870-0169-d1e7-e053-2995a90ad3edad152870-0168-d1e7-e053-2995a90ad3ed2020-08-17WarningsExact identifier
spl id: ad152870-0169-d1e7-e053-2995a90ad3ed
spl set id: ad152870-0168-d1e7-e053-2995a90ad3ed

Reported adverse events (FAERS/openFDA)#

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