FDA.reportPublic FDA data

Delphis Eco

Manufacturer
DELPHIS ECO LIMITED
Effective date
2021-02-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:35

Label at a glance#

ProductDelphis Eco Hand Sanitising Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Hand sanitiser to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces. Should be applied regularly. 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

Benzalkonium Chloride 3.0% (w/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitiser to help reduce bacteria that potentially can cause disease.
  • For use when soap and water are not available.

Warning

WARNINGS SECTION

  • For external use only.

OTC - DO NOT USE SECTION

Do not use

  • on 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. Do not ingest. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

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.
  • Should be applied regularly.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information or Comments

STORAGE AND HANDLING SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis, Cocamide DEA, Cocamine Oxide, Didecyldimonium chloride, Fragrance, Propylene glycol, Water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Delphis Eco Hand Sanitiser (100 mL) NDC: 81560-001-01

Hand Sanitizer 100 mLHand Sanitizer 100 mL

Delphis Eco Hand Sanitising Spray (500 mL) NDC: 81560-002-05

Hand Sanitising Spray 500 mLHand Sanitising Spray 500 mL

Delphis Eco Hand Sanitising Spray (700 mL) NDC: 81560-002-07

Hand Sanitising Spray 700 mLHand Sanitising Spray 700 mL

Delphis Eco Hand Sanitising Foam (5 L) NDC: 81560-003-50

Hand Sanitising Foam 5 LHand Sanitising Foam 5 L

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2480125benzalkonium chloride 3 % Topical FoamPSN1
2480126benzalkonium chloride 3 % Topical SprayPSN1
2480125benzalkonium chloride 30 MG/ML Topical FoamSCD1
2480126benzalkonium chloride 30 MG/ML Topical SpraySCD1
2480125benzalkonium chloride 3 % Topical FoamSY1
2480126benzalkonium chloride 3 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81560-001-012023-01-30C16284748780-1f386c649-d001-0266-e053-dadaa90a7c1aDelphis Eco Hand Sanitiser
81560-002-052023-01-30C16284748780-1f386c649-d001-0266-e053-dadaa90a7c1aDelphis Eco Hand Sanitiser
81560-002-072023-01-30C16284748780-1f386c649-d001-0266-e053-dadaa90a7c1aDelphis Eco Hand Sanitiser
81560-003-502023-01-30C16284748780-1f386c649-d001-0266-e053-dadaa90a7c1aDelphis Eco Hand Sanitiser

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81560-001-01Delphis EcoHand Sanitiser100 mL in 1 BOTTLELIQUID1001
81560-002-05Delphis Eco500 mL in 1 BOTTLE, SPRAYLIQUID5001
81560-002-07Delphis Eco700 mL in 1 BOTTLE, SPRAYLIQUID7001
81560-003-50Delphis EcoHand Sanitising Foam5000 mL in 1 BOTTLELIQUID50001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81560-001DELPHIS ECO HAND SANITISING FOAM (BENZALKONIUM CHLORIDE) LIQUID DELPHIS ECO (BENZALKONIUM CHLORIDE) LIQUID DELPHIS ECO HAND SANITISER (BENZALKONIUM CHLORIDE) LIQUID [DELPHIS ECO LIMITED]1Legacy NDC, 1 package rows20210227_ba9a6122-b059-2358-e053-2995a90a43d4.zip
81560-002DELPHIS ECO HAND SANITISING FOAM (BENZALKONIUM CHLORIDE) LIQUID DELPHIS ECO (BENZALKONIUM CHLORIDE) LIQUID DELPHIS ECO HAND SANITISER (BENZALKONIUM CHLORIDE) LIQUID [DELPHIS ECO LIMITED]1Legacy NDC, 2 package rows20210227_ba9a6122-b059-2358-e053-2995a90a43d4.zip
81560-003DELPHIS ECO HAND SANITISING FOAM (BENZALKONIUM CHLORIDE) LIQUID DELPHIS ECO (BENZALKONIUM CHLORIDE) LIQUID DELPHIS ECO HAND SANITISER (BENZALKONIUM CHLORIDE) LIQUID [DELPHIS ECO LIMITED]1Legacy NDC, 1 package rows20210227_ba9a6122-b059-2358-e053-2995a90a43d4.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81560-00181560-001-01
81560-00281560-002-07, 81560-002-05
81560-00381560-003-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
COCAMINE OXIDEQWA2IZI6FIIACT
COCO DIETHANOLAMIDE92005F972DIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
COCAMINE OXIDEQWA2IZI6FIIACT
COCO DIETHANOLAMIDE92005F972DIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
COCAMINE OXIDEQWA2IZI6FIIACT
COCO DIETHANOLAMIDE92005F972DIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT

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
ba9a6122-b05a-2358-e053-2995a90a43d4ba9a6122-b059-2358-e053-2995a90a43d42021-02-25WarningsExact identifier
spl id: ba9a6122-b05a-2358-e053-2995a90a43d4
spl set id: ba9a6122-b059-2358-e053-2995a90a43d4

Reported adverse events (FAERS/openFDA)#

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