FDA.reportPublic FDA data

State Street Eucalyptus Hand Sanitizer Antiseptic

Manufacturer
Redi-2-Paq Home Products, LLC
Effective date
2022-07-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:56:04

Label at a glance#

ProductState Street Eucalyptus Hand Sanitizer Antiseptic
Active ingredientALCOHOL
Label structure2 sections

Label contents#

Full prescribing information#

Drug Facts

SPL UNCLASSIFIED SECTION

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

Hand Sanitizer helps reduce bacteria that may cause disease.

External use only. Flammable.

WARNINGS SECTION

Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

  • On children less than 2 months of age
  • On open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears and mouth. In case of contact with eyes, rinse thoroughly with water.

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

  • Place product on hands to cover all exposed surfaces. Rub hands together until dry.
  • Supervise children under age 6 to prevent ingestion of sanitizer.

Other information

OTHER SAFETY INFORMATION

  • store between 15-30 °C (59-86 °F)
  • Avoid freezing and excessive heat above 40 °C (104 °F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Isopropyl alcohol, Polysorbate 20, Carbomer, Triethanolamine, Glycerin, Isopropyl myristate, Tocopheryl acetate, Parfum, Lilia, Benzyl Salicylate, Hexyl cinnamal, Alpha-isomethyl ionone.

Questions?

OTC - QUESTIONS SECTION

Visit penta5usa.com or Call Toll Free 1-800-511-5609

State Street Eucalyptus Hand Sanitizer Ethyl Alcohol Antiseptic 70%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72697-100472697-1004-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
POLYSORBATE 207T1F30V5YHIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
BENZYL SALICYLATEWAO5MNK9TUIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
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
e4174bbd-b20b-2e21-e053-2995a90ac488f60ea742-5196-447f-8697-a8a358a2449c2022-07-18WarningsExact identifier
spl id: e4174bbd-b20b-2e21-e053-2995a90ac488
spl set id: f60ea742-5196-447f-8697-a8a358a2449c

Reported adverse events (FAERS/openFDA)#

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