FDA.reportPublic FDA data

Refresh Foaming Instant Hand Sanitizer

Manufacturer
Evonik Stockhausen, LLC
Effective date
2011-10-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:29:57

Label at a glance#

ProductRefresh Foaming Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethanol (68%)

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Kills harmful bacteria that can be found on the skin.

WARNINGS SECTION

Flammable. For external use only. Avoid contact with eyes.
In case of accidental eye contact, flush eyes thoroughly with water.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if skin or eye irritation persists for more than 72 hours..

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.

DOSAGE & ADMINISTRATION SECTION

Pump product in palm of hand and rub thoroughly until hands are dry. Do not rinse or wipe off foam.

INACTIVE INGREDIENT SECTION

Deionized water, Bis-PEG/PPG-20/20 Dimethicone, ethylcellulose, PEG-14M

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Stoko Refresh

Instant Hand Sanitizer Foam

NPN 80005750

Imported by / Importe par:

Trans Canada Distribution Inc.,

Mississauga, ON L5L 5Y7

Net Contents 33.8 fl.oz.

Contenu Net: 1000ml

Manufactured in USA

Fabrique aux E-U.

Stoko Skin Care

Evonik Stockhausen, LLC

Greensboro, NC 27406

1-800-334-0242 www.StokoSkinCare.com

Stock #/No De Stock: 35231

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Refresh Foam Label 050 04Refresh Foam Label 050 04

OTC - STOP USE SECTION

Discontinue use if irritation and redness develops.

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1191684ethanol 68 % Topical FoamPSN1
1191684ethanol 0.68 ML/ML Topical FoamSCD1
1191684ethanol 68 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64064-050-042019-11-13C16284748780-197449f38-c40d-f6ea-e053-dbdaa90aa703Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64064-050-04Refresh Foaming Instant Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICLIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64064-050REFRESH FOAMING INSTANT HAND SANITIZER (ALCOHOL) LIQUID [EVONIK STOCKHAUSEN, LLC]1Legacy NDC, 1 package rows20111101_ad02b319-4b1c-49e1-9c76-44ed35e21c78.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1
ETHYLCELLULOSESINACTIVE INGREDIENT7Z8S9VYZ4B1
POLYETHYLENE GLYCOL 14000INACTIVE INGREDIENT77HY82S0LG1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
64064-05064064-050-04

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
POLYETHYLENE GLYCOL 1400077HY82S0LGIACT
ETHYLCELLULOSES7Z8S9VYZ4BIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 14 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BGRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL1000 mgExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BTABLET, EXTENDED RELEASE / ORAL1120 mgExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BTABLET / ORAL300 mgExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BCREAM / TOPICALNAExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BTABLET, FILM COATED, EXTENDED RELEASE / ORAL52.5 mgExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BTABLET, FILM COATED / ORAL83 mgExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BSYSTEM / TOPICAL10 mgExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BCAPSULE, EXTENDED RELEASE / ORAL153 mgExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BSUSPENSION, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BCAPSULE / ORAL12.32 mgExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BTABLET, COATED / ORAL20 mgExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BPOWDER, FOR SUSPENSION / ORALNAExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BTABLET, DELAYED RELEASE / ORAL53.8 mgExact identifier — unii candidate
14 equally ranked IID candidates
ETHYLCELLULOSESETHYLCELLULOSE7Z8S9VYZ4BPOWDER / ORAL2090 mgExact identifier — unii candidate
14 equally ranked IID candidates

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
ad02b319-4b1c-49e1-9c76-44ed35e21c78ad02b319-4b1c-49e1-9c76-44ed35e21c782011-10-26WarningsExact identifier
spl id: ad02b319-4b1c-49e1-9c76-44ed35e21c78
spl set id: ad02b319-4b1c-49e1-9c76-44ed35e21c78

Reported adverse events (FAERS/openFDA)#

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