ActiveClean OTC Spray Hand Sanitizer

Manufacturer
CleanSpot, Inc.
Effective date
2016-12-12
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 22:48:09

Label at a glance#

ProductActiveClean
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Shake container. Use enough product to throughly cover hands. Rub hands together briskly until dry. Children under 6 use only with adult supervision.

WARNINGS SECTION

For External Use only. Flammable. Keep away from fire or flame.When using the product, do not use it in or near the eyes. In case of contact, rinse eyes throughly with water. Stop use and ask a doctor if irritation or rash appears and lasts. If swallowed get medical help or contact a PoisonControl Center right away.

INACTIVE INGREDIENT SECTION

water, isopropyl alcohol (rubbing alcohol), beeswax, apricit seed oil, tocopherol (Vitamin E), essential oils of lemon and peppermint,(epsilon) - polylysine

OTC - PURPOSE SECTION

Antimicrobial

OTC - ACTIVE INGREDIENT SECTION

Ethanol 62% v/v

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria on skin that could cause disease
  • Recommended for repeated use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71012-111-602020-01-31C16284748780-19d75b9cf-ece1-f424-e053-dadaa90a57ceActiveClean OTC Spray Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71012-111-60ActiveClean1 in 1 CONTAINERAEROSOL, SPRAY18
71012-111-60ActiveClean3 mL in 1 BOTTLE, SPRAYAEROSOL, SPRAY38

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71012-111ACTIVECLEAN (ETHANOL SDA 3C 200) AEROSOL, SPRAY [CLEANSPOT, INC.]8Legacy NDC, 2 package rows20161212_3e213095-134b-0679-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71012-11171012-111-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
437ae79b-69a3-1985-e054-00144ff8d46c3e213095-134b-0679-e054-00144ff88e882016-12-12WarningsExact identifier
spl id: 437ae79b-69a3-1985-e054-00144ff8d46c
spl set id: 3e213095-134b-0679-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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