Victis

Manufacturer
Yield Scientific Llc
Effective date
2020-04-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:15

Label at a glance#

ProductVictis Active Defense Essential
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other Information ▪ Store between 15-30°C (59-86°F). ▪ Avoid Freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% 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 ▪ in children under 2 months of age ▪ on open skin wounds

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

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions ▪ 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.

STORAGE AND HANDLING SECTION

Other Information ▪ Store between 15-30°C (59-86°F). ▪ Avoid Freezing and excessive heat above 40°C (104°F)

INACTIVE INGREDIENT SECTION

Inactive Ingredients glycerin, hydrogen peroxide, purified water USP

SPL UNCLASSIFIED SECTION

WHO/CDC Approved Formulation Designed for 99.99% Germ-Killing Effectiveness*

▪ Topical Solution ▪ Non-Sterile Solution

*Kills 99.99% of most common germs that may cause illness

Distributed by

Yield Scientific LLC, 220 Outlet Pointe

Blvd, Columbia, SC 29210

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76803-180-01VictisActive Defense Essential50 mL in 1 BOTTLE, PLASTICSOLUTION501
76803-180-02VictisActive Defense Essential375 mL in 1 BOTTLE, PLASTICSOLUTION3751
76803-180-03VictisActive Defense Essential3785 mL in 1 JUGSOLUTION37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76803-180VICTIS ACTIVE DEFENSE ESSENTIAL (ALCOHOL) SOLUTION [YIELD SCIENTIFIC LLC]1Legacy NDC, 3 package rows20200502_54da1109-a2a2-4b2e-8f5f-2670f0a3045c.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76803-18076803-180-01, 76803-180-02, 76803-180-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
8f09f7a9-3555-4005-908e-09d12fa5d76054da1109-a2a2-4b2e-8f5f-2670f0a3045c2020-04-29WarningsExact identifier
spl id: 8f09f7a9-3555-4005-908e-09d12fa5d760
spl set id: 54da1109-a2a2-4b2e-8f5f-2670f0a3045c

Reported adverse events (FAERS/openFDA)#

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