DEFENSE AG DISINFECTANT- ea disinfectant spray spray

Defense AG Disinfectant by

Drug Labeling and Warnings

Defense AG Disinfectant by is a Otc medication manufactured, distributed, or labeled by Nexderma. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 80% v/v. Purpose: Antiseptic to help reduce bacteria that potentially can cause disease.

Inactive ingredients

hydrogen peroxide, ultra pure water, Nano Silver Ag+

Use

To clean and remove allergens, wipe surfaces clean with product and let dry. Can use on porous surfaces. Kills 99.99% of germs around the home, office and classroom.

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.

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

Directions

• Spray enough product to cover all surfaces. Wipe clean and let it dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Purpose

Antiseptic to help reduce bacteria that potentially can cause disease.

Package Label - Principal Display Panel

473 mL NDC: 79930-7109-4

946 mL NDC: 79930-7109-6

3790 mL NDC: 79930-7109-5

INGREDIENTS AND APPEARANCE

DEFENSE AG DISINFECTANT 
ea disinfectant spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79930-7109
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SILVER (UNII: 3M4G523W1G)	0.2 mL  in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.125 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79930-7109-4	473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/01/2020
2	NDC: 79930-7109-6	946 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/01/2020
3	NDC: 79930-7109-5	3790 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/01/2020

Labeler - Nexderma (079533940)

Establishment
Name	Address	ID/FEI	Business Operations
Nexderma		079533940	manufacture(79930-7109) , pack(79930-7109) , label(79930-7109)