FDA.reportPublic FDA data

Eco Sanitizer Liquid

Manufacturer
0966452 B.C. Ltd.
Effective date
2020-10-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:46

Label at a glance#

ProductEco Sanitizer Liquid
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Store between 15° C/59° F and 30° C/86° F

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Purpose: Antiseptic

INDICATIONS & USAGE SECTION

Use: Hand sanitizer to help reduce bacteria on skin

DOSAGE & ADMINISTRATION SECTION

Directions for Use: Supervise children when they use this product. For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to dry. 

OTC - ACTIVE INGREDIENT SECTION

Medicinal Ingredients: Ethyl Alcohol* (80% v/v).

INACTIVE INGREDIENT SECTION

Ingredients: Aqua, Glycerin*, Hydrogen Peroxide*.

WARNINGS SECTION

Warning: For external use only. Flammable. Keep away from open flame and sources of heat. Avoid contact with eyes. Should this occur, flush eyes with water. If irritation develops, discontinue use and contact a health care practitioner.

Contraindications: Do not use on children/infants less than 2 years of age (unless directed by a health care practitioner).

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

STORAGE AND HANDLING SECTION

Store between 15° C/59° F and 30° C/86° F

SPL UNCLASSIFIED SECTION

kills 99.9% of germs

Get your hands on it !

Fragrance free | Hypoallergenic 

Enriched Liquid with Glycerin | Can be used as is or as a refill

Made in Canada from Domestic and imported products.

Eco Sanitizer | ecosanitizer.ca

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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80731-001-012023-01-30C16284748780-1f386c649-ca51-0266-e053-dadaa90a7c1aeco HAND SANITIZER LIQUID
80731-001-022023-01-30C16284748780-1f386c649-ca51-0266-e053-dadaa90a7c1aeco HAND SANITIZER LIQUID
80731-001-032023-01-30C16284748780-1f386c649-ca51-0266-e053-dadaa90a7c1aeco HAND SANITIZER LIQUID
80731-001-042023-01-30C16284748780-1f386c649-ca51-0266-e053-dadaa90a7c1aeco HAND SANITIZER LIQUID

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80731-001-01Eco Sanitizer Liquid50 mL in 1 BOTTLELIQUID501
80731-001-02Eco Sanitizer Liquid355 mL in 1 BOTTLELIQUID3551
80731-001-03Eco Sanitizer Liquid1000 mL in 1 BOTTLELIQUID10001
80731-001-04Eco Sanitizer Liquid4000 mL in 1 BOTTLELIQUID40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80731-001ECO SANITIZER LIQUID (ETHYL ALCOHOL) LIQUID [0966452 B.C. LTD.]1Legacy NDC, 4 package rows20201017_8a6cf506-988e-42c0-8428-8a34196263e8.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
80731-00180731-001-01, 80731-001-02, 80731-001-03, 80731-001-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT

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
5f62ed18-7552-4fff-b62c-0d05f209983f8a6cf506-988e-42c0-8428-8a34196263e82020-10-12WarningsExact identifier
spl id: 5f62ed18-7552-4fff-b62c-0d05f209983f
spl set id: 8a6cf506-988e-42c0-8428-8a34196263e8

Reported adverse events (FAERS/openFDA)#

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