FDA.reportPublic FDA data

Moor Spa Hand Sanitizing

Manufacturer
Bodywell Natural Skin Ca re Inc | Bodywell Natural Skin Care Inc
Effective date
2023-01-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:40:11

Label at a glance#

ProductMoor Spa Hand Sanitizing
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand Sanitizer to Help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Spray enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 year of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to Help reduce bacteria that potentially can cause disease. For use
when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

    Do not use

  • in children less than 2 months of age   
  • on open skin or wounds.

When using this product keep out of eyes, ears and mouth. In case of contact with eyes,
rinse thoroughly with water.
Stop use and ask a doctor if irritation occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, call a Poison Control Center or get medical help right away. 

Directions

DOSAGE & ADMINISTRATION SECTION

Spray enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 year of age when using this product to avoid swallowing.

Other Information.

SPL UNCLASSIFIED SECTION

  • Store between 15-30 °C (59-86 °F)

• Avoid freezing & excessive heat above 40°C (104°F)

Inactive Ingredients.

INACTIVE INGREDIENT SECTION

Aqua, Aloe Barbadensis (Aloe Vera) Leaf Juice, Glycerin, D Alpha Tocopherol (Vitamin E), Western Red Cedar (Thuja Plicata) Leaf Oil

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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
81441-00881441-008-01, 81441-008-02, 81441-008-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
THUJA PLICATA LEAFR9I752FESHIACT
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
2a301487-6dcb-d367-e063-6394a90a236bedb1f705-e812-492e-8443-b62409f08b702024-12-26WarningsExact identifier
spl set id: edb1f705-e812-492e-8443-b62409f08b70

Reported adverse events (FAERS/openFDA)#

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