NuuxSan Instant Hand Sanitizer

Manufacturer
Albek de Mexico, S.A. de C.V.
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:28

Label at a glance#

ProductNuuxSan Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

hand sanitizer to help decrease bacteria on the skin when water, soap & towel are not aviable recommended for repeated use.

Dosage and administration

use as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help decrease bacteria on the skin
  • when water, soap & towel are not aviable recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

Do not apply arround eyes.

Do not use

OTC - DO NOT USE SECTION

in ears & mouth

Stop use and ask a doctor if

OTC - STOP USE SECTION

ittitation and redness develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • use as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Other information

SPL UNCLASSIFIED SECTION

  • Shore al 20°C (68° to 77°F).
  • May discolor fabrics.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

water, carbomer, triethnolamine, glycerin, propylene glycol, fragrance, aloe barbadensis leaf juice.

Package Labeling:100 ML

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:500 ML

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

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
72758-003-002022-01-28C16284748780-1d6a99b39-f459-a426-e053-dadaa90af4c2NuuxSan Instant Hand Sanitizer
72758-003-012022-01-28C16284748780-1d6a99b39-f459-a426-e053-dadaa90af4c2NuuxSan Instant Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72758-003-00NuuxSan Instant Hand Sanitizer100 mL in 1 BOTTLELIQUID1001
72758-003-01NuuxSan Instant Hand Sanitizer500 mL in 1 BOTTLELIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72758-003NUUXSAN INSTANT HAND SANITIZER (ALCOHOL) LIQUID [ALBEK DE MEXICO, S.A. DE C.V.]1Legacy NDC, 2 package rows20200609_4afffbfa-6a53-4ec2-bf15-b373b401a229.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72758-00372758-003-00, 72758-003-01

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
a797ac76-cf7e-d91b-e053-2995a90a099e4afffbfa-6a53-4ec2-bf15-b373b401a2292020-06-08WarningsExact identifier
spl id: a797ac76-cf7e-d91b-e053-2995a90a099e
spl set id: 4afffbfa-6a53-4ec2-bf15-b373b401a229

Reported adverse events (FAERS/openFDA)#

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