FDA.reportPublic FDA data

Eco Sun Moisturizing Spray Hand Sanitizer

Manufacturer
Eco Sun Naturals, LLC
Effective date
2021-05-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:45:21

Label at a glance#

ProductEco Sun Moisturizing Hand Sanitizer
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

to help reduce bacteria on the skin

Dosage and administration

Spray onto hands, wetting thoroughly with product. Rub into skin until dry. Children under 6 years of age should be supervised by an adult when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 64%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat and flame.

When using this product

OTC - WHEN USING SECTION

avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray onto hands, wetting thoroughly with product. Rub into skin until dry.
  • Children under 6 years of age should be supervised by an adult when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water (Aqua), Aloe Barbadensis Leaf Juice*, Propanediol, Citrus Limonum Oil, Eugenia Caryophyllus Bud Oil, Eucalyptus Globulus Leaf Oil, Rosmarinus Officinalis Leaf Oil, Cinnamomum Zeylanicum Bark Oil, Camellia Sinensis Leaf Extract* *Organic

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90063-00390063-003-02

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
LEMON OILI9GRO824LLIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
PROPANEDIOL5965N8W85TIACT
EUCALYPTUS OIL2R04ONI662IACT
ROSEMARY OIL8LGU7VM393IACT
CINNAMON BARK OILXE54U569ECIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
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
0a2222f3-efaa-e854-e063-6394a90aa0a1b3713421-ca5e-223e-e053-2a95a90a2f3c2023-11-14WarningsExact identifier
spl set id: b3713421-ca5e-223e-e053-2a95a90a2f3c

Reported adverse events (FAERS/openFDA)#

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