DEFENSE AG DISINFECTANT- disinfectant spray spray
Nexderma

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Defense AG Disinfectant ISO - New

Active Ingredient(s)

Isopropyl Alcohol 75% v/v. Purpose: Antiseptic to help reduce bacteria that potentially can caused disease.

Hydrogen Peroxide

Inactive ingredients

ultra pure water, Nano Silver Ag+

Use

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

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

Antisepticbto help reduce bacteria that potentially can cause disease.

Package Label - Principal Display Panel

473 ml NDC: 79930-7115-4

ISO 16 Oz Label

946 ml NDC: 79930-7115-6

ISO 32 Oz Label

3.79 L NDC: 79930-7115-5

ISO 32 Oz Label

DEFENSE AG DISINFECTANT
disinfectant spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79930-7115
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	0.125 mL in 100 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL in 100 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:79930-7115-4	473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/09/2020
2	NDC:79930-7115-6	946 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/09/2020
3	NDC:79930-7115-5	3790 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/09/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	11/09/2020

Labeler - Nexderma (079533940)

Name	Address	ID/FEI	Business Operations
Establishment
Nexderma		079533940	manufacture(79930-7115) , pack(79930-7115) , label(79930-7115)

Revised: 11/2020

Document Id: b3c5e553-ea12-2f85-e053-2995a90a1437

Set id: b3c5e21b-7683-3115-e053-2a95a90a8fdd

Version: 1

Effective Time: 20201104

Nexderma