NANO MINI I DO hand sanitizer

Manufacturer
DISINFEKT ENVIRONMENTAL SOLUTIONS FZE
Effective date
2020-12-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:35:33

Label at a glance#

ProductNANO MINI I DO hand sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

wet hands thoroughly with product and to dry without wiping • children under 6 years of ages should be supervised when using this product. • Not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol    70%

Purpose

OTC - PURPOSE SECTION

Antiseptic.

Use [s]

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on the skin that could cause disease.
  • recommended for repeated use.

Warnings

WARNINGS SECTION

  • For external use only
  • Flammable, keep away from fire or flame
  • Do not use  in or near the eyes

When using this product keep out of eyes, ears, and mouth.

  • In case of contact with eyes, rinse eyes thoroughly with water rinse eyes thoroughly with water

Stop use and ask a doctor if

  • irritation and redness develop.
  • condition persists for more than 72 hours.

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

  • wet hands thoroughly with product and to dry without wiping

• children under 6 years of ages should be supervised when using this product.

• Not recommended for infants.

Other information

SPL UNCLASSIFIED SECTION

  • Avoid freezing and excessive heat above 104º F (40º C).
  • Store between 15-30º C (59-86 ºF)
  • When exposed to light, liquid solution color may very without effecting the effectiveness of formula.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera, Fragrance (parfum), Glycerin, Grape Seed Oil, Isopropyl Myristate, Propylene glycol, Water

PRODUCT IMAGE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81231-004-012023-01-30C16284748780-1f386c649-b824-0266-e053-dadaa90a7c1aNANO MINI I DO

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81231-004-01NANO MINI I DO hand sanitizer45 mL in 1 CONTAINERLIQUID451

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81231-004NANO MINI I DO HAND SANITIZER (ETHYL ALCOHOL) LIQUID [DISINFEKT ENVIRONMENTAL SOLUTIONS FZE]1Legacy NDC, 1 package rows20201219_2d5e9b9c-5ec2-405f-a73e-e511c2be0551.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81231-00481231-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
b6c9e6bc-e07a-5e20-e053-2a95a90ac4a42d5e9b9c-5ec2-405f-a73e-e511c2be05512020-12-18WarningsExact identifier
spl id: b6c9e6bc-e07a-5e20-e053-2a95a90ac4a4
spl set id: 2d5e9b9c-5ec2-405f-a73e-e511c2be0551

Reported adverse events (FAERS/openFDA)#

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