1.8OZ ARMSTRONG HAND SANITIZER WITH ALOE VERA AND VITAMIN E- alcohol gel

1.8oz Armstrong Hand Sanitizer with Aloe Vera and Vitamin E by

Drug Labeling and Warnings

1.8oz Armstrong Hand Sanitizer with Aloe Vera and Vitamin E by is a Otc medication manufactured, distributed, or labeled by BLUE CROSS LABORATORIES, INC., NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Kills Over 99% of Most Common Germs within seconds

Armstrong allows you to wash your hands whenever conventional soap and water is not available. Use as an aid to reduce exposure to infectious germs and to supplement daily handwashing. Helps meet U.S. Government standards by protecting against exposure to bloodborne diseases. Nontozic-For External Use Only.

Keep bottle of Armstrong in

• Kitchen Medical Offices Nurseries
• Automobile Bathrooms Workplace

Drug Facts Active Ingredients

Ethyl Alcohol 65%

Purpose

Antimicrobial

Directions:

• Put a thumbnail size amount in your palm and rub your hands together briskly until dry.
• Children 6 years of age should be supervised when using Armstrong.

Inactive Ingredients:

Water (Aqua),Aloe Barbadensis Leaf Juice, Carbomer,Fragrance,Glycerin,Propylene Glycol,Tocopheryl Acetate,Triethanolamine.

Warning

• Flammable, keep away from flame.
• Keep out of eyes. In case of eye contact immediately flush eyes with water then contact physician.
• If swallowed, contact physician.
• For External Use Only.
• Do not store above 110℉。

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

1.8oz Armstrong Hand Sanitizer

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

1.8OZ ARMSTRONG HAND SANITIZER WITH ALOE VERA AND VITAMIN E 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	33 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-020-01	53 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/25/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/25/2017

Labeler - BLUE CROSS LABORATORIES, INC. (008298879)

Registrant - NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. (530766098)

Establishment
Name	Address	ID/FEI	Business Operations
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.		530766098	manufacture(22431-020)