ARMICARE HAND SANITIZER- alcohol liquid

ArmiCare Hand Sanitizer by

Drug Labeling and Warnings

ArmiCare Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Armis Biopharma, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

ACTIVE INGREDIENT

Ethyl Alcohol 75% v/v.

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

• On children less than 2 months of age
• On open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222

Directions:

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

Other information:

• Store between 15-30C (59-86F )
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients:

Deionized water, Glycerin, Hydrogen Peroxide, Acetic Acid, Lavender, Polysorbate-20

QUESTIONS?

1-800-970-1779

Package Labeling:

Package Labeling:

INGREDIENTS AND APPEARANCE

ARMICARE HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81793-187
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
ACETIC ACID (UNII: Q40Q9N063P)
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81793-187-00	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/05/2021
2	NDC: 81793-187-03	89 mL in 1 TUBE; Type 0: Not a Combination Product	02/12/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/05/2021

Labeler - Armis Biopharma, Inc (166990189)