FDA.reportPublic FDA data

Sanitiz Advanced Hand Sanitizer

Manufacturer
Tecnoglobal Ph7, S.a. De C.v.
Effective date
2020-04-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:07

Label at a glance#

ProductSanitiz Advanced Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. 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(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in 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. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, hydrogen peroxide, glycerin, carbomer, aminomethylpropanol, phenoxyethanol/Iodopropynyl butylcarbamate, tetrasodium EDTA, ext. violet 2, aloe barbadensis leaf juice

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

251 mL NDC: 75470-100-01

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN1
1041498ethanol 0.8 ML/ML Topical GelSCD1
1041498ethanol 80 % Topical GelSY1

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
75470-100-012022-01-28C16284748780-1d6a99b39-3b48-a426-e053-dadaa90af4c2a3ba38a5-d901-1176-e053-2995a90a0d38
75470-100-022022-01-28C16284748780-1d6a99b39-3b48-a426-e053-dadaa90af4c2a3ba38a5-d901-1176-e053-2995a90a0d38
75470-100-032022-01-28C16284748780-1d6a99b39-3b48-a426-e053-dadaa90af4c2a3ba38a5-d901-1176-e053-2995a90a0d38

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75470-100-01Sanitiz Advanced Hand Sanitizer251 mL in 1 BOTTLEGEL2511
75470-100-02Sanitiz Advanced Hand Sanitizer400 mL in 1 BOTTLEGEL4001
75470-100-03Sanitiz Advanced Hand Sanitizer900 mL in 1 BOTTLEGEL9001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75470-100SANITIZ ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [TECNOGLOBAL PH7, S.A. DE C.V.]1Legacy NDC, 3 package rows20200421_a3ba38a5-d901-1176-e053-2995a90a0d38.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75470-10075470-100-01, 75470-100-02, 75470-100-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
EDETATE SODIUMMP1J8420LUIACT
ALOE VERA LEAFZY81Z83H0XIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
EXT. D&C VIOLET NO. 2G5UX3K0728IACT
CARBOMER 9404Q93RCW27EIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
ALCOHOL3K9958V90MACTIB

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
a3ba2e76-545e-3d6e-e053-2a95a90a6e4ca3ba38a5-d901-1176-e053-2995a90a0d382020-04-20WarningsExact identifier
spl id: a3ba2e76-545e-3d6e-e053-2a95a90a6e4c
spl set id: a3ba38a5-d901-1176-e053-2995a90a0d38

Reported adverse events (FAERS/openFDA)#

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