HAND SANITIZER WITH ALOE AND VITAMIN E- ethyl alcohol liquid

Hand Sanitizer with Aloe and Vitamin E by

Drug Labeling and Warnings

Hand Sanitizer with Aloe and Vitamin E by is a Otc medication manufactured, distributed, or labeled by Top's Healthcare Product Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Antibacterial Hand Sanitizer

​Active Ingredient

Ethyl Alcohol 71% (V/V)

Purpose​

Antiseptic

Features:

To decrease bacteria on the skin. Recommended for repeated use. Delicate and fast dry. Use anywhere without water.

Inactive Ingredients:

Water (Aqua), Isopropyl Alcohol, Glycerin, Aloe Yohyju Matsu Ekisu, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Fragrance (Parfum).

Directions:

• Place enough product in your palm to thoroughly cover your hands.
• Rub hands together briskly until dry.
• Children under 8 years of age should be supervised when using this product.

Warning:

• Flammable. Keep away from fire or flame.
• For external use only.
• When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
• Stop using and ask a doctor, if irritation or rash appears and lasts.

• Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Other information:

• Do not store above 110°F (43°C).
• May discolor certain fabrics or surfaces.

SPL UNCLASSIFIED SECTION

Kills 99.99% of Germs

Distributor: Tops Healthcare Product Inc.

2233 E 49th Street, Vernon 90058 CA, USA     THP

E-mail: customerservice@topshealthcare.com

Production Date: Please find on the package

Shelf life: 2 years

Executive Standard: GB 26373

Made in China

Packaging

INGREDIENTS AND APPEARANCE

HAND SANITIZER WITH ALOE AND VITAMIN E 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75227-151
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75227-151-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
2	NDC: 75227-151-03	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
3	NDC: 75227-151-05	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
4	NDC: 75227-151-10	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/26/2020

Labeler - Top's Healthcare Product Inc (117482389)