FDA.reportPublic FDA data

Cleanology Advanced Hand Sanitizer

Manufacturer
Southern Telecom, Inc.
Effective date
2020-05-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:31:57

Label at a glance#

ProductCleanology Advanced Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USE:

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only, do not inhale or ingest.

Do not use

OTC - DO NOT USE SECTION

in, or near the eyes. In case of contact with eyes, rinse thoroughly with water.

Avoid contact with broken skin

Stop use and ask a doctor if 

OTC - STOP USE SECTION

irritation or rash develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry without wiping.
  • For children under 6, use only under adult supervision.
  • Not recommended for infants.

Other information

SPL UNCLASSIFIED SECTION

  • Store below 110°F (43°C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, acrylate/C10-30, alkyl acrylate crosspolymer, benzophenone-4, fragrance, glycerin, tocopherol

Package Labeling:76546-000-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug FactsDrug FactsFrontFront

Package Labeling:76546-000-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60mL Label60mL Label

Package Labeling:76546-000-03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

300mL Label300mL Label

Package Labeling:76546-000-04

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500mL Label500mL Label

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76546-00076546-000-01, 76546-000-02, 76546-000-03, 76546-000-04

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
WATER059QF0KO0RIACT
SULISOBENZONE1W6L629B4KIACT
GLYCERINPDC6A3C0OXIACT
TOCOPHEROLR0ZB2556P8IACT
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
a7a882f7-5a8a-09f2-e053-2995a90af7d46b586e4b-cb2e-40d9-a23a-2cff9cd9e18a2020-06-09WarningsExact identifier
spl set id: 6b586e4b-cb2e-40d9-a23a-2cff9cd9e18a

Reported adverse events (FAERS/openFDA)#

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