Scentia Hand Sanitizer

Manufacturer
Laboratorios Quimico Farmaceuticos Lancasco SA
Effective date
2020-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:21:43

Label at a glance#

ProductScentia Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Apply a sufficient amount of product on your hands and rub until completely dry. Repeat if necessary.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70%

Purpose

OTC - PURPOSE SECTION

Antibacterial 

Use

INDICATIONS & USAGE SECTION

for hand sanitizer to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

Flammable

When using this product

OTC - WHEN USING SECTION

Avoid contact with the eyes and mouth.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation and redness appear.

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 immediately..

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply a sufficient amount of product on your hands and rub until completely dry. Repeat if necessary.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Isopropyl alcohol, Aqua, quanternary ammonium, glicerine. May contain: carbomer, hydoxyethylcellulose, triethanolamine.

Package Labeling:300 ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Package Labeling:1.0L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Package Labeling:5L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5Label5

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79103-001SCENTIA HAND SANITIZER (ALCOHOL) GEL [LABORATORIOS QUIMICO FARMACEUTICOS LANCASCO SA]1Legacy NDC20200714_aa52eb32-1ab4-d3ba-e053-2995a90a234e.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79103-00179103-001-03, 79103-001-04, 79103-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
48682280-4024-e432-e063-6394a90ae235aa52eb32-1ab4-d3ba-e053-2995a90a234e2026-01-15WarningsExact identifier
spl set id: aa52eb32-1ab4-d3ba-e053-2995a90a234e

Reported adverse events (FAERS/openFDA)#

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