Remote refresh instant hand sanitizer wipe

Manufacturer
Greenhouse Agency, Inc.
Effective date
2021-05-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:44:25

Label at a glance#

ProductRemote refresh instant hand sanitizer wipe
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

for hand sanitizing to decrease bacteria on skin recommended for repeated use

Dosage and administration

tear open packet, remove wipe  Wet hands thoroughly with product and let hands air dry  throw used wipe in trash do not flush

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Propose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • for hand sanitizing to decrease bacteria on skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Flammable:keep away from fire of flame

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes, if in eyes, flush thoroughly with water

When Discontinue use and contact a doctor if

OTC - ASK DOCTOR SECTION

irritation and redness develop and conditions persist for more than 72 hours

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

unless under adult supervision. if swallowed,get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • tear open packet, remove wipe 
  • Wet hands thoroughly with product and let hands air dry 
  • throw used wipe in trash do not flush

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Tocopheryl Acetate

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Package
Outer Package

Inner PackageInner Package

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81727-00081727-000-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB

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
d9a4c456-8543-9805-e053-2995a90ab243c32ba1da-84d5-1551-e053-2995a90a7a8e2022-03-07WarningsExact identifier
spl set id: c32ba1da-84d5-1551-e053-2995a90a7a8e

Reported adverse events (FAERS/openFDA)#

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