![1.8OZ ARMSTRONG HAND SANITIZER WITH ALOE VERA AND VITAMIN E (ALCOHOL) GEL [BLUE CROSS LABORATORIES, INC.]](https://medic.hrt.org//dailymed/images/5d759a16-840d-6257-e053-2a91aa0ab808/1.8oz Armstrong Hand Sanitizer.jpg)
| NDC | 22431-020-01 |
| Set ID | 5d759a16-840d-6257-e053-2a91aa0ab808 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | BLUE CROSS LABORATORIES, INC. |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | PART333A |
- 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
- Purpose
- 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.
Close - 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
- INGREDIENTS AND APPEARANCE
1.8OZ ARMSTRONG HAND SANITIZER WITH ALOE VERA AND VITAMIN E
alcohol gelProduct 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) CloseEstablishment Name Address ID/FEI Business Operations NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. 530766098 manufacture(22431-020)