FDA.reportPublic FDA data

SKINSEI

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-11-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:35:52

Label at a glance#

ProductSKINSEI
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use

Dosage and administration

• Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. Recommended for repeated use.

Label contents#

Full prescribing information#

SKINSEI HAND SANITIZER - Alcohol liquid

DESCRIPTION SECTION

Skinsei Hand Sanitizer

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame
For external use only
Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.
When using this product avoid contact with eyes · In case of contact, flush eyes with water, call a doctor · Avoid contact with broken skin

Do not drink. Not edible.
In case of accidental ingeston seek professional assistance or contact a Poison Contro Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
Children should only use this product under adult supervision

Directions

DOSAGE & ADMINISTRATION SECTION

• Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. Recommended for repeated use.

Other information

OTHER SAFETY INFORMATION

• Do not store above 104˚F (40˚C). May discolor some fabrics · harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Carthamus Tinctorius (Safflower) Oleosomes, Polyacrylate Cross Polymer - 6 Hydroxyethyl Cellulose, Glycerin.

OTC - QUESTIONS SECTION

(800) 621-2079.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SkinseiHandSanitizerSkinseiHandSanitizer

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
64942-1740-12024-11-07C16284748780-11030e365-3aea-111a-e063-dadaa90a10e2Skinsei Hand Sanitizer
64942-1740-12024-01-30C16284748780-11030e365-3aea-111a-e063-dadaa90a10e2Skinsei Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1740-1SKINSEI118 mL in 1 CONTAINERLIQUID1183

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1740SKINSEI (ETHYL ALCOHOL LIQUID) LIQUID [CONOPCO INC. D/B/A/ UNILEVER]3Current NDC, Legacy NDC, 1 package rows20241109_a603c419-238f-0bae-e053-2a95a90abc2b.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
64942-174064942-1740-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
CARTHAMUS TINCTORIUS SEED OLEOSOMES9S60Q72309IACT

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
SKINSEIETHYL ALCOHOL LIQUIDConopco Inc. d/b/a/ Unilevera603c419-238f-0bae-e053-2a95a90abc2b2024-11-07WarningsExact identifier
ndc (package): 64942-1740-1
ndc (product): 64942-1740
ndc11 (package): 64942174001
spl id: 2656edda-0ae0-4ed5-e063-6394a90ae9ca
spl set id: a603c419-238f-0bae-e053-2a95a90abc2b

Reported adverse events (FAERS/openFDA)#

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