Decon-E Antiseptic Hand Sanitizer

Manufacturer
Maverick Abrasives Corporation
Effective date
2022-01-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:47:47

Label at a glance#

ProductDecon-E Antiseptic Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

hand sanitizer to decrease bacteria on the skin recommended for repeated use for use when soap and water are not available

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

store between 15-30 ° C (59-86 ° F) avoid freezing and excessive heat above 40 ° C (104 ° F) 3-25 heat seal enclosure

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to decrease bacteria on the skin
  • recommended for repeated use
  • for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame

For external use only

Do not use

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

When using this product 

  • do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

  • irritation and redness develop
  • condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and allow to dry without wiping
  • supervise children under 6 years of age when using this product to avoid swallowing

Other information

STORAGE AND HANDLING SECTION

  • store between 15-30 °C (59-86 °F)
  • avoid freezing and excessive heat above 40 °C (104 °F)
  • 3-25 heat seal enclosure

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, tert-Butyl Alcohol, Hydrogen Peroxide, Eucalyptus Oil, Orange ( Citrus sinensis) Oil, Lemon Oil, Lime Oil, Grapefruit ( Citrus paradisi) Oil

Questions?

OTC - QUESTIONS SECTION

+1-714-604-1469

You may also report serious side effects to this phone number. Mon-Fri 9:00AM-5:00 PM

SPL UNCLASSIFIED SECTION

NON-STERILE SOLUTION

ESSENTIAL OILS FRAGRANCE

70% ETHYL ALCOHOL

APPLY AND LET DRY

WARNING SEE SIDE PANEL

DESCRIPTION

Renegade Home & Business Decon-E is a non-sterile, antiseptic hand sanitizer. Solutions with an ethyl alcohol content of 70% are known and proven to be effective in decreasing bacteria. Fresh and citrusy, our Decon hand sanitizer is effective in decontaminating your skin. This skin-softening formula also contains 100% pure, therapeutic-grade essential oils.

MADE IN THE U.S.A

Manufactured by: Maverick Abrasives, 4340 E Miraloma Ave.,
Anaheim, CA 92807

For more ingredient information visit:
www.RenegadeProductsUSA.com or call
TF: [800] 276-5474

WARNING

Cancer and Reproductive Harm

www.P65Warnings.ca.gov

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73837-652-16Decon-E Antiseptic Hand Sanitizer474 mL in 1 BOTTLESOLUTION4742

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73837-652DECON-E ANTISEPTIC HAND SANITIZER (ETHYL ALCOHOL) SOLUTION [MAVERICK ABRASIVES CORPORATION]2Legacy NDC, 1 package rows20220130_b72233bf-af3c-4b46-a618-e4ae1dbcea57.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73837-65273837-652-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
d6b1c2b9-0f20-88a5-e053-2a95a90a1639b72233bf-af3c-4b46-a618-e4ae1dbcea572022-01-28WarningsExact identifier
spl id: d6b1c2b9-0f20-88a5-e053-2a95a90a1639
spl set id: b72233bf-af3c-4b46-a618-e4ae1dbcea57

Reported adverse events (FAERS/openFDA)#

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