FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Tecnoglobal Ph7, S.a. De C.v. | Tecnoglobal Ph7 S.a De C.v.
Effective date
2020-08-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:25:46

Label at a glance#

ProductHand 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 70% 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.

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, PEG-12 Dimethicone, Glycerin, Carbomer, Propylene Glycol, Aminomethyl Propanol, Phenoxyethanol, Iodoprpynyl Butylcarbamate, Tetrasodium EDTA, Ext. Violet 2, Aloe Barbadensis Leaf Juice

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30mL NDC: 75470-110-05

60mL NDC: 75470-110-04

900mL NDC: 75470-110-03

110-03110-03

400mL NDC: 75470-110-02

110-02110-02

251mL NDC: 75470-110-01

LABEL 1LABEL 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN3
582753ethanol 0.7 ML/ML Topical SolutionSCD3
582753ethanol 70 % Topical SolutionSY3
582753ethyl alcohol 70 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75470-110-012022-01-28C16284748780-1d6a99b39-faa4-a426-e053-dadaa90af4c2Sanitz 75470-110
75470-110-022022-01-28C16284748780-1d6a99b39-faa4-a426-e053-dadaa90af4c2Sanitz 75470-110
75470-110-032022-01-28C16284748780-1d6a99b39-faa4-a426-e053-dadaa90af4c2Sanitz 75470-110
75470-110-042022-01-28C16284748780-1d6a99b39-faa4-a426-e053-dadaa90af4c2Sanitz 75470-110
75470-110-052022-01-28C16284748780-1d6a99b39-faa4-a426-e053-dadaa90af4c2Sanitz 75470-110

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75470-110-01Hand Sanitizer251 mL in 1 BOTTLELIQUID2513
75470-110-02Hand Sanitizer400 mL in 1 BOTTLELIQUID4003
75470-110-03Hand Sanitizer900 mL in 1 BOTTLELIQUID9003
75470-110-04Hand Sanitizer60 mL in 1 BOTTLELIQUID603
75470-110-05Hand Sanitizer30 mL in 1 BOTTLELIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75470-110HAND SANITIZER (ALCOHOL) LIQUID [TECNOGLOBAL PH7, S.A. DE C.V.]3Legacy NDC, 5 package rows20200826_aaf1900c-a4c1-e4a8-e053-2a95a90a2a14.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
75470-11075470-110-01, 75470-110-02, 75470-110-03, 75470-110-04, 75470-110-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9404Q93RCW27EIACT
PHENOXYETHANOLHIE492ZZ3TIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
EXT. D&C VIOLET NO. 2G5UX3K0728IACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
PEG-12 DIMETHICONEZEL54N6W95IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAFZY81Z83H0XIACT
EDETATE SODIUMMP1J8420LUIACT

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
adb48ee7-000f-6631-e053-2a95a90ae0d6aaf1900c-a4c1-e4a8-e053-2a95a90a2a142020-08-25WarningsExact identifier
spl id: adb48ee7-000f-6631-e053-2a95a90ae0d6
spl set id: aaf1900c-a4c1-e4a8-e053-2a95a90a2a14

Reported adverse events (FAERS/openFDA)#

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