MOXE CITRUS HAND SANITIZER- alcohol gel

MOXE Citrus Hand Sanitizer by

Drug Labeling and Warnings

MOXE Citrus Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Be Moxe, LLC, JW Nutritional, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Ethyl Alcohol 70% by volume

Purpose

Antiseptic

Uses

Use to help reduce bacteria on the skin.

Warnings

• For external use only.
• Flammable.
• Keep away from fire or flame.

Do Not Use Near Eyes.

In case of contact, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor

If skin irritation develops

Keep Out Of Reach Of Children.

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

Directions

• Place sanitizer on palm, rub hands together.
• Supervise children under 6.

Other Information

Do not store over 110° F

Questions?

Call 1-800-296-3160

Inactive Ingredients

Water, Carbomer, Glycerin, Aloe Leaf Juice, Tocopheryl Acetate, Fragrance

SPL UNCLASSIFIED SECTION

Distributed by:
Be MOXĒ LLC 4700 140th Ave N., Ste 112,
Clearwater, FL 33762

PRINCIPAL DISPLAY PANEL - 118 ml Bottle Label

MOXĒ

CITRUS

HAND
SANITIZER

70% Alcohol

MADE IN
USA

4FL OZ | 118ml

INGREDIENTS AND APPEARANCE

MOXE CITRUS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75435-813
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)
Carbomer Homopolymer, Unspecified Type (UNII: 0A5MM307FC)
Glycerin (UNII: PDC6A3C0OX)
Aloe (UNII: V5VD430YW9)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75435-813-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020
2	NDC: 75435-813-08	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020
3	NDC: 75435-813-12	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020
4	NDC: 75435-813-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	06/17/2020

Labeler - Be Moxe, LLC (114624756)

Establishment
Name	Address	ID/FEI	Business Operations
JW Nutritional, LLC		017642837	MANUFACTURE(75435-813)