MOOR SPA HAND SANITIZING- ethanol liquid

Moor Spa Hand Sanitizing by

Drug Labeling and Warnings

Moor Spa Hand Sanitizing by is a Otc medication manufactured, distributed, or labeled by Bodywell Natural Skin Ca re Inc, Bodywell Natural Skin Care Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug facts

Active ingredient

Ethanol 70%

Purpose

Antiseptic

Uses

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

Warnings

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.

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

Directions

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.

• Store between 15-30 °C (59-86 °F)

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

Inactive Ingredients.

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

Product label

INGREDIENTS AND APPEARANCE

MOOR SPA HAND SANITIZING 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81441-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
THUJA PLICATA LEAF (UNII: R9I752FESH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81441-008-01	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/07/2021
2	NDC: 81441-008-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/07/2021
3	NDC: 81441-008-03	3800 mL in 1 DRUM; Type 0: Not a Combination Product	05/07/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/07/2021

Labeler - Bodywell Natural Skin Ca re Inc (201162026)

Establishment
Name	Address	ID/FEI	Business Operations
Bodywell Natural Skin Care Inc		201162026	manufacture(81441-008)