DEFENSE ZONE HAND SANITIZER- ethyl alcohol spray

Defense Zone by

Drug Labeling and Warnings

Defense Zone by is a Otc medication manufactured, distributed, or labeled by Prime Packaging, Prime Enterprises. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

to decrease bacteria on the skin that could cause disease. recommrnded for repeated use

Warning

For external use only

Dot not use

Do not use on damaged or broken skin

When using this product

Keep away from face to avoid breathing it. Keep out of eyes. rinse with water to remove.

Stop use and ask a doctor

If irritation and redness occurs if condition persistes for more than 72 hours.

Keep out of reach of children

If product is swallowed, get medical help or contact a Posion Control Center right away.

Flammable

Avoid fire, flame, heat and smoking. Contents under pressre. do not punture or incinerate. Store at temperatures below 120°F(50°C).

Directions

wet hands thoroughly with product and allow to dry without wiping. for children under 6, use only under adult supervision. not recommended for infants.

Other Information

do not store above 104°F. may discolor some fabrics. harmful to wood finishes and plastics.

Inactive ingredients

Aloe Barbadensis Leaf Juice,Glycerin,Isopropyl Myristate, Tocopherol,Water.

Questions

Call 1 855-548-4653

Principal display label

INGREDIENTS AND APPEARANCE

DEFENSE ZONE  HAND SANITIZER
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 13630-0161
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Product Characteristics
Color	white (Clear)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 13630-0161-4	177 mL in 1 CAN; Type 0: Not a Combination Product	09/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/21/2020

Labeler - Prime Packaging (805987059)

Registrant - Prime Packaging (805987059)

Establishment
Name	Address	ID/FEI	Business Operations
Prime Enterprises		101946028	analysis(13630-0161) , manufacture(13630-0161)

Establishment
Name	Address	ID/FEI	Business Operations
Prime Packaging		805987059	label(13630-0161) , pack(13630-0161)