FDA.reportPublic FDA data

Stoko Refresh Foaming Instant Hand Sanitizer

Manufacturer
SC Johnson Professional USA, Inc. | NWL Netherlands Production B.V.
Effective date
2021-01-28
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:54:26

Label at a glance#

ProductStoko Refresh Foaming Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision.

Storage and handling

Do not store above 105°F (40°C). May discolor certain fabrics or surfaces. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 68% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Flammable: Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • Avoid contact with broken skin.
  • Do not inhale or ingest.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition 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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry without wiping.
  • For children under 6, use only under adult supervision.

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 105°F (40°C).
  • May discolor certain fabrics or surfaces.
  • Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized water, Bis-PEG/PP G-20/20 Dimethicone, Ethylcellulose, PEG-14M

Questions?

OTC - QUESTIONS SECTION

800-248-7190 (Mon - Fri, 8 am - 5 pm EST)

PRINCIPAL DISPLAY PANEL - 800 ml Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SCJ PROFESSIONAL
A Family Company™

NDC 11084-958-53

STOKO® REFRESH

Foaming Instant Hand Sanitizer

deb
SKIN CARE

PRINCIPAL DISPLAY PANEL - 800 ml Bottle Carton
PRINCIPAL DISPLAY PANEL - 800 ml Bottle Carton

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
11084-95811084-958-53, 11084-958-77

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
BIS-PEG/PPG-20/20 DIMETHICONE05W209DSBSIACT
ETHYLCELLULOSE (50 MPA.S)6I475159RAIACT
POLYETHYLENE OXIDE 6000002126FD486LIACT

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
07b5e7ad-3e3f-40e0-acc5-a072f7b977060f53e343-6c7d-4f1e-b3ec-0d19aea109182022-12-21WarningsExact identifier
spl set id: 0f53e343-6c7d-4f1e-b3ec-0d19aea10918

Reported adverse events (FAERS/openFDA)#

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