MOOR SPA HAND SANITIZING- ethanol liquid 
Bodywell Natural Skin Ca re Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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

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.

• 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

image descriptionimage description

image description

MOOR SPA HAND SANITIZING 
ethanol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81441-008
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)  
THUJA PLICATA LEAF (UNII: R9I752FESH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81441-008-01120 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2021
2NDC:81441-008-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2021
3NDC:81441-008-033800 mL in 1 DRUM; Type 0: Not a Combination Product05/07/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/07/2021
Labeler - Bodywell Natural Skin Ca re Inc (201162026)
Establishment
NameAddressID/FEIBusiness Operations
Bodywell Natural Skin Care Inc201162026manufacture(81441-008)

Revised: 1/2023
Document Id: f2773fc2-8ad7-2ba7-e053-2a95a90a6cfc
Set id: edb1f705-e812-492e-8443-b62409f08b70
Version: 2
Effective Time: 20230117
 
Bodywell Natural Skin Ca re Inc