FDA.reportPublic FDA data

Raw Sugar Hand Sanitizer Eucalyptus and Tea Tree

Manufacturer
Bolero Home Decor, Inc.
Effective date
2021-10-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:34:17

Label at a glance#

ProductRaw Sugar Hand Sanitizer Eucalyptus and Tea Tree
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizing to reduce bacteria on the skin that could cause disease  Recommended for repeated use 

Dosage and administration

Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under the age of 6 should be supervised when using this product

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizing to reduce bacteria on the skin that could cause disease 
  • Recommended for repeated use 

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.
For external use only. Do not inhale or ingest.

Avoid contact with eyes. In case of eye contact, fush eyes with water.

Stop use and see a doctor if

OTC - STOP USE SECTION

  • irritation or redness develops 
  • condition persists 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to thoroughly cover your hands
  • Rub hands together briskly until dry
  • Children under the age of 6 should be supervised when using this product

Other Information

SPL UNCLASSIFIED SECTION

  • Store at 20-25°C (68-77°F) 
  • May discolor certain fabrics or surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Carbomer, Aminomethyl Propanol, Glycerin, *Eucalyptus Globulus Leaf Extract, Melaleuca Alternifolia (Tea Tree) Flower/Leaf/Stem Extract, *Aloe Barbadensis (Aloe Vera) Leaf Juice, Geraniol, Linalool, Limonene, Fragrance (Parfum) *Certified Organic

Package Labeling:59ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 mL59 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

266 mL266 mL

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57469-07157469-071-01, 57469-071-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
GLYCERINPDC6A3C0OXIACT
EUCALYPTUS GLOBULUS LEAFS546YLW6E6IACT
MELALEUCA ALTERNIFOLIA FLOWERING TOP5AZ4S6N66FIACT
ALOE VERA LEAFZY81Z83H0XIACT
GERANIOLL837108USYIACT
LINALOOL, (+/-)-D81QY6I88EIACT
LIMONENE, (+)-GFD7C86Q1WIACT
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
cd88b6b0-bf51-0c5a-e053-2995a90aa121b2937c52-cc0c-a832-e053-2a95a90a42592021-10-04WarningsExact identifier
spl id: cd88b6b0-bf51-0c5a-e053-2995a90aa121
spl set id: b2937c52-cc0c-a832-e053-2a95a90a4259

Reported adverse events (FAERS/openFDA)#

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