Cleanslate Hand Sanitizer

Manufacturer
Cleanslate Group LLC
Effective date
2023-02-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:36:17

Label at a glance#

ProductCleanslate Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

to decrease bacteria on the skin after changing diapers, assisting ill persons, or before contact with a person under medical care or treatment.

WARNINGS SECTION

Warnings

For external use only.

Flammable, keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last 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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

  • apply liberally to hands to cover all surfaces, including the area under the fingernails
  • rub hands together until dry

INACTIVE INGREDIENT SECTION

Inactive Ingredients benzalkonium chloride, chlorhexidine gluconate, isopropyl alcohol, PEG-10 dimethicone, phenoxyethanol, polyethylene oxide 600000, polyquaternium 10, water.

SPL UNCLASSIFIED SECTION

MFD FOR CLEANSLATE GROUP LLC

1420 EAST LINDEN AVENUE

LINDEN, NJ 07036

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cleanslate

HAND SANITIZER

ALCOHOL 70%

33.8 fl. oz. (1000mL)

80586-21280586-212

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80586-212-102023-02-19C16284748780-1f386c649-f777-0266-e053-dadaa90a7c1aCleanslate Hand Sanitizer
80586-212-102023-01-30C16284748780-1f386c649-f777-0266-e053-dadaa90a7c1aCleanslate Hand Sanitizer

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80586-21280586-212-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
f51648c1-1d55-edf8-e053-2a95a90ac881d102cd71-a891-c8d6-e053-2a95a90aff3f2023-02-19WarningsExact identifier
spl id: f51648c1-1d55-edf8-e053-2a95a90ac881
spl set id: d102cd71-a891-c8d6-e053-2a95a90aff3f

Reported adverse events (FAERS/openFDA)#

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