FDA.reportPublic FDA data

Scentia Hand Sanitizer

Manufacturer
Laboratorios Quimico-Farmaceuticos Lancasco, S.A.
Effective date
2020-12-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:59:37

Label at a glance#

ProductScentia Hand Sanitizer
Active ingredientALCOHOL
Label structure6 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, quaternary ammonium, glicerin. May contain: carbomer, hydroxyethylcellulose, triethanolamine.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79103-003-012026-01-15C16284748780-11030e365-05c8-111a-e063-dadaa90a10e2Scentia Hand Sanitizer
79103-003-012024-01-30C16284748780-11030e365-05c8-111a-e063-dadaa90a10e2Scentia Hand Sanitizer

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79103-003SCENTIA HAND SANITIZER (ALCOHOL) GEL [LABORATORIOS QUIMICO-FARMACEUTICOS LANCASCO, S.A.]1Legacy NDC20201230_b57d6e5d-bb64-1d96-e053-2995a90aca2a.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79103-00379103-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
ISOPROPYL ALCOHOLND2M416302IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT

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
4868574c-e168-fc1f-e063-6294a90a76f3b57d6e5d-bb64-1d96-e053-2995a90aca2a2026-01-15WarningsExact identifier
spl set id: b57d6e5d-bb64-1d96-e053-2995a90aca2a

Reported adverse events (FAERS/openFDA)#

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