FDA.reportPublic FDA data

ECO Hand Sanitizer

Manufacturer
ECO AERONAUTICS INC
Effective date
2020-06-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:59

Label at a glance#

ProductECO Hand Sanitizer
Active ingredientALCOHOL
Label structure9 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

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% 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 less than 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 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

Sodium Hydroxide, Solvent Green 3, Acrylates Copolymer , purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79173-001-012022-01-28C16284748780-1d6a99b39-5b50-a426-e053-dadaa90af4c2b7ab9dc8-74f1-41b0-a2d3-d07437a6cbc5
79173-001-022022-01-28C16284748780-1d6a99b39-5b50-a426-e053-dadaa90af4c2b7ab9dc8-74f1-41b0-a2d3-d07437a6cbc5
79173-001-032022-01-28C16284748780-1d6a99b39-5b50-a426-e053-dadaa90af4c2b7ab9dc8-74f1-41b0-a2d3-d07437a6cbc5
79173-001-042022-01-28C16284748780-1d6a99b39-5b50-a426-e053-dadaa90af4c2b7ab9dc8-74f1-41b0-a2d3-d07437a6cbc5
79173-001-052022-01-28C16284748780-1d6a99b39-5b50-a426-e053-dadaa90af4c2b7ab9dc8-74f1-41b0-a2d3-d07437a6cbc5
79173-001-062022-01-28C16284748780-1d6a99b39-5b50-a426-e053-dadaa90af4c2b7ab9dc8-74f1-41b0-a2d3-d07437a6cbc5
79173-001-072022-01-28C16284748780-1d6a99b39-5b50-a426-e053-dadaa90af4c2b7ab9dc8-74f1-41b0-a2d3-d07437a6cbc5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79173-001-01ECO Hand Sanitizer100 mL in 1 BOTTLEGEL1001
79173-001-02ECO Hand Sanitizer200 mL in 1 BOTTLEGEL2001
79173-001-03ECO Hand Sanitizer350 mL in 1 BOTTLEGEL3501
79173-001-04ECO Hand Sanitizer450 mL in 1 BOTTLEGEL4501
79173-001-05ECO Hand Sanitizer1000 mL in 1 BOTTLEGEL10001
79173-001-06ECO Hand Sanitizer3785 mL in 1 BOTTLEGEL37851
79173-001-07ECO Hand Sanitizer50 mL in 1 BOTTLEGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79173-001ECO HAND SANITIZER (ALCOHOL) GEL [ECO AERONAUTICS INC]1Legacy NDC, 7 package rows20200625_b7ab9dc8-74f1-41b0-a2d3-d07437a6cbc5.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
79173-00179173-001-01, 79173-001-02, 79173-001-03, 79173-001-04, 79173-001-05, 79173-001-06, 79173-001-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
SODIUM HYDROXIDE55X04QC32IIACT
D&C GREEN NO. 64QP5U84YF7IACT
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%)2N8MDB79NAIACT
WATER059QF0KO0RIACT

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
877f3b05-d15c-4956-b4ab-32e1b1fb729cb7ab9dc8-74f1-41b0-a2d3-d07437a6cbc52020-06-23WarningsExact identifier
spl id: 877f3b05-d15c-4956-b4ab-32e1b1fb729c
spl set id: b7ab9dc8-74f1-41b0-a2d3-d07437a6cbc5

Reported adverse events (FAERS/openFDA)#

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