AMOVEO ORIGINAL- alcohol gel

Amoveo Original by

Drug Labeling and Warnings

Amoveo Original by is a Otc medication manufactured, distributed, or labeled by Protair-X Health Solutions Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Alcohol 80%

Purpose

Antiseptic

Uses

• For handwashing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

For external use only.
Flammable, keep away from fire or flame.

Do not use

in the eyes

Stop use and ask a doctor if:

• irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

• Wet hands thoroughly with product and allow to dry without wiping

Other Information

• avoid temperatures over 110°F
• may discolor certain fabrics
• harmful to wood finishes and plastics

Inactive Ingredients

Aloe Vera, Carbomer, Fragrance, Glycerin, Tocopheryl Acetate, Triethanolamine, Water

Questions?

Call 1 - 877 - 874 - 0606 Weekdays, 9AM – 5PM EST

Package Labeling:

INGREDIENTS AND APPEARANCE

AMOVEO ORIGINAL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49955-701
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	700 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49955-701-50	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/24/2017
2	NDC: 49955-701-01	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/24/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/24/2017

Labeler - Protair-X Health Solutions Inc. (205614519)