ZONE DEFENSE FOAMING HAND SANITIZER- alcohol liquid

Zone Defense Foaming Hand Sanitizer by

Drug Labeling and Warnings

Zone Defense Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Baer Enterprises, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethanol 62% v/v. Purpose: Antiseptic

Isopropyl Alcohol 5% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

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 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 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.

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

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

Directions

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

Other information

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

Inactive ingredients

Water, Polyethylene Glycol Dimethicone, Caprylyl Glycol, Isopropyl Myristate, Glycerin, Tocopheryl Acetate

Package Label - Principal Display Panel

18 fl. oz. (532 mL) NDC: 73829-101-18

INGREDIENTS AND APPEARANCE

ZONE DEFENSE FOAMING HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73829-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	5 mL  in 100 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CAPRYLYL GLYCOL (UNII: 00YIU5438U)	1 mL  in 100 mL
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)	5 mL  in 100 mL
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	0.5 mL  in 100 mL
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)	1 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	25 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73829-101-18	532 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/16/2020

Labeler - Baer Enterprises, LLC (189728590)

Registrant - Baer Enterprises, LLC (189728590)

Establishment
Name	Address	ID/FEI	Business Operations
Baer Enterprises, LLC		189728590	manufacture(73829-101)