FDA.reportPublic FDA data

Sanaux Hand Sanitizer Antibacterial Gel

Manufacturer
SANLOZ GROUP INC. | SANLOZ MATERIALES AVANZADOS S.A.P.I. DE C.V.
Effective date
2020-04-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:02

Label at a glance#

ProductSanaux Hand Sanitizer Antibacterial Gel
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand sanitizer to help reduce bacteria on skin.

Dosage and administration

Place enough product in your palm to thoroughly cover both hands. Rub hand together briskly until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antibacterial   

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

Keep out of reach of children.

When using this product, do not use in or near the eyes. In case of exposure in eyes wash thoroughly with lots of water.

If swallowed do not attempt to induce vomit, seek medical attention or contact poison control center immediately.

This product is intended for external use only. Flammable. Keep away from fire or flame.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly cover both hands. Rub hand together briskly until dry. Children under 6 years of age should be supervised when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Carboxymethylcellulose, Triethanolamine, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 01Label 01Label 03Label 03Label 02Label 02Label 04Label 04Label 05Label 05Label 07Label 07

Label 06Label 06

Label 08Label 08

Label 09Label 09

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
75509-001-012022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-022022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-032022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-042022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-052022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-062022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-072022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-082022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-092022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-102022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-112022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-122022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-132022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-142022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40
75509-001-152022-01-28C16284748780-1d6a99b39-be15-a426-e053-dadaa90af4c2744262e6-025c-467f-88ce-3e559797ca40

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75509-001-01Sanaux Hand Sanitizer Antibacterial Gel30 mL in 1 TUBEGEL301
75509-001-02Sanaux Hand Sanitizer Antibacterial Gel50 mL in 1 TUBEGEL501
75509-001-03Sanaux Hand Sanitizer Antibacterial Gel60 mL in 1 TUBEGEL601
75509-001-04Sanaux Hand Sanitizer Antibacterial Gel100 mL in 1 TUBEGEL1001
75509-001-05Sanaux Hand Sanitizer Antibacterial Gel200 mL in 1 TUBEGEL2001
75509-001-06Sanaux Hand Sanitizer Antibacterial Gel240 mL in 1 TUBEGEL2401
75509-001-07Sanaux Hand Sanitizer Antibacterial Gel250 mL in 1 TUBEGEL2501
75509-001-08Sanaux Hand Sanitizer Antibacterial Gel500 mL in 1 TUBEGEL5001
75509-001-09Sanaux Hand Sanitizer Antibacterial Gel900 mL in 1 TUBEGEL9001
75509-001-10Sanaux Hand Sanitizer Antibacterial Gel1000 mL in 1 TUBEGEL10001
75509-001-11Sanaux Hand Sanitizer Antibacterial Gel1890 mL in 1 TUBEGEL18901
75509-001-12Sanaux Hand Sanitizer Antibacterial Gel3780 mL in 1 TUBEGEL37801
75509-001-13Sanaux Hand Sanitizer Antibacterial Gel18900 mL in 1 TUBEGEL189001
75509-001-14Sanaux Hand Sanitizer Antibacterial Gel200000 mL in 1 TUBEGEL2000001
75509-001-15Sanaux Hand Sanitizer Antibacterial Gel1000000 mL in 1 TUBEGEL10000001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75509-001SANAUX HAND SANITIZER ANTIBACTERIAL GEL (ALCOHOL) GEL [SANLOZ GROUP INC.]1Legacy NDC, 15 package rows20200421_744262e6-025c-467f-88ce-3e559797ca40.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
75509-00175509-001-01, 75509-001-02, 75509-001-03, 75509-001-04, 75509-001-05, 75509-001-06, 75509-001-07, 75509-001-08, 75509-001-09, 75509-001-10, 75509-001-11, 75509-001-12, 75509-001-13, 75509-001-14, 75509-001-15

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
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
CARBOXYMETHYLCELLULOSE05JZI7B19XIACT

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
e1bdae16-c2be-46b5-b64c-9dd4b0a65d10744262e6-025c-467f-88ce-3e559797ca402020-04-15WarningsExact identifier
spl id: e1bdae16-c2be-46b5-b64c-9dd4b0a65d10
spl set id: 744262e6-025c-467f-88ce-3e559797ca40

Reported adverse events (FAERS/openFDA)#

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