Imunology Sanitizer

Manufacturer
World Health Products, LLC | Tropical Enterprises International
Effective date
2020-07-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:11

Label at a glance#

ProductImunology Sanitizer
Active ingredientAlcohol
Label structure10 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

Wet hand thoroughly with product and allow to dry without wiping.

Storage and handling

Non-staining, may discolor certain fabrics.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

WARNINGS

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If contact with eyes occurs, flush with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, seek prompt medical attention.

STORAGE AND HANDLING SECTION

Flammable. Keep away from open flame. Do not store above 110° F.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hand thoroughly with product and allow to dry without wiping.

Other information

STORAGE AND HANDLING SECTION

Non-staining, may discolor certain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Fragrance.

Questions

OTC - QUESTIONS SECTION

1-800-535-5053

PRINCIPAL DISPLAY PANEL - 89 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

THE PROTECTION BRAND

Imūnology™

SANITIZER

Maximum Strength
Anti-Bacterial

3 fl oz (89ml)

DEVELOPED BY
GAT®
SPORT
DEVELOPED BY

Principal Display Panel - 89 ml Bottle Label
Principal Display Panel - 89 ml Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79636-003-252022-01-28C16284748780-1d6a99b39-5e9b-a426-e053-dadaa90af4c2Imūnology™ Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79636-003-25Imunology Sanitizer89 mL in 1 BOTTLELIQUID891
79636-003-25Imunology Sanitizer1 in 1 BOXLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79636-003IMUNOLOGY SANITIZER (ALCOHOL) LIQUID [WORLD HEALTH PRODUCTS, LLC]1Legacy NDC, 2 package rows20200808_b45f3b69-a87d-47aa-a058-adad5be6d54b.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
79636-00379636-003-25

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
c955dd2f-2eee-4b08-b650-2640c248dc91b45f3b69-a87d-47aa-a058-adad5be6d54b2020-07-27WarningsExact identifier
spl id: c955dd2f-2eee-4b08-b650-2640c248dc91
spl set id: b45f3b69-a87d-47aa-a058-adad5be6d54b

Reported adverse events (FAERS/openFDA)#

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