eQo Gel

Manufacturer
INTERNATIONAL HARBOR LLC | Octapod, S.A. de C.V.
Effective date
2020-09-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:29:25

Label at a glance#

ProducteQo Gel
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 to avoid swallowing.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

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

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

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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 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 to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, carbomer, triethanolamine.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP 3785 ml NDC:79838-002-01 PDP 3785 mLPDP 3785 mL

PDP 250 ml NDC:79838-002-02 PDP 250 mlPDP 250 ml

PDP 500 ml NDC:79838-002-03 PDP 500 mlPDP 500 ml

PDP 1000 ml NDC:79838-002-04 PDP 1000 ml gelPDP 1000 ml gel

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79838-002-01eQo Gel3785 mL in 1 BOTTLEGEL37852
79838-002-02eQo Gel250 mL in 1 BOTTLEGEL2502
79838-002-03eQo Gel500 mL in 1 BOTTLEGEL5002
79838-002-04eQo Gel1000 mL in 1 BOTTLEGEL10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79838-002EQO GEL (ALCOHOL) GEL [INTERNATIONAL HARBOR LLC]2Legacy NDC, 4 package rows20200916_adbb2029-c51e-2384-e053-2995a90af28d.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79838-00279838-002-02, 79838-002-03, 79838-002-04, 79838-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
af5dc601-72b2-ea45-e053-2a95a90a2bb0adbb2029-c51e-2384-e053-2995a90af28d2020-09-15WarningsExact identifier
spl id: af5dc601-72b2-ea45-e053-2a95a90a2bb0
spl set id: adbb2029-c51e-2384-e053-2995a90af28d

Reported adverse events (FAERS/openFDA)#

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