1.8OZ ARMSTRONG HAND SANITIZER WITH ALOE VERA AND VITAMIN E- alcohol gel
BLUE CROSS LABORATORIES, 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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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.

1.8oz Armstrong Hand Sanitizer

label

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

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

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

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

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

Labeler - BLUE CROSS LABORATORIES, INC. (008298879)

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

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