Eagle Promotions

Manufacturer
Nutrix International, LLC.
Effective date
2020-05-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:14

Label at a glance#

ProductEagle Promotions
Active ingredientALCOHOL
Label structure12 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 avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

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

OTC - WHEN USING SECTION

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

Stop use

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 avoid swallowing.

Other Information

OTHER SAFETY INFORMATION

  • Store between 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C (104°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Propylene Glycol, Glycerin, Methyl Hydroxypropyl Cellulose, Melaleuca Alternifolia (Tea Tree) Leaf Oil.

Purpose

OTC - PURPOSE SECTION

PurposePurposeAntiseptic

Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Full Package label Package labelPackage label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73333-284-012022-01-28C16284748780-1d6a99b39-c147-a426-e053-dadaa90af4c2a62f0288-49c8-64dd-e053-2995a90a075a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73333-284-01Eagle Promotions284 g in 1 BOTTLEGEL2841

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73333-284EAGLE PROMOTIONS (INSTANT HAND SANITIZER GEL) GEL [NUTRIX INTERNATIONAL, LLC.]1Legacy NDC, 1 package rows20200522_a62f0288-49c8-64dd-e053-2995a90a075a.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
73333-28473333-284-01

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
a62ea769-88c1-71c2-e053-2a95a90a64a8a62f0288-49c8-64dd-e053-2995a90a075a2020-05-21WarningsExact identifier
spl id: a62ea769-88c1-71c2-e053-2a95a90a64a8
spl set id: a62f0288-49c8-64dd-e053-2995a90a075a

Reported adverse events (FAERS/openFDA)#

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