HAND SANITIZER- ethanol liquid

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Bell Food & Beverage Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient(s)

Ethanol 75% v/v. Purpose, Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use(s)

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 heat or flame.

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth.

In case of contact with eyes, rinse eyes throughly with water.

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

STOP USE

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

• Plave enough product on hands to cover all surfaces.
• Rub hands together until dry.
• Supervise children under 6 years of age when using this ptoduct.

Other Information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

glycerin, hydrogen perioxide, xantham gum, distilled water

Principal Display Label

473 ml NDC: 73806-0002-1

236ml NDC: 73806-0002-2

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73806-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
XANTHAN GUM (UNII: TTV12P4NEE)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73806-0002-1	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
2	NDC: 73806-0002-2	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/22/2020

Labeler - Bell Food & Beverage Inc (081550987)

Establishment
Name	Address	ID/FEI	Business Operations
Bell Food & Beverage Inc		081550987	manufacture(73806-0002)