HAND SANITIZER- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Amazon Services LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Use

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 fire 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. 

Directions

• Apply entire contents of pouch onto hands and rub briskly until dry.
• Children under 6 years of age should be supervised when using this product.

Other information:

• Store below 110°F (43°C)
• May discolor certain fabrics and surfaces

Inactive Ingredients

Alicyle Acrylate, Aminomethyl, Caprylyl Glycol, Crosspolymer, Fragrance, Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Propanol, Tocopherol Acetate, Water(Aqua)

Questions?:

800-719-9260

Package Labeling:

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72288-196
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYL ALCOHOL (UNII: 96F264O9SV)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72288-196-01	6 in 1 BOX	06/14/2021
1		160 in 1 CARTON
1		1.2 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/14/2021

Labeler - Amazon Services LLC (128990418)