DEFENSE AG HAND SANITIZER- ipa hand sanitizer gel

Defense AG Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient(s)

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

Inactive ingredients

Ultra Pure Water, Hydroxyethyl Cellulose, Curcumin

Purpose

To help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are unavailable.

Warnings

Keep away form fire and flame.
Flammable
For external use on hands only.
Keep out of eye, ears and mouth.
If contact in eyes, flush thoroughly with water.
Keep out of reach of children.
If swallowed seek medical help immediately or call your poison control center.
Store between 15-30 (58-86F)
Avoid freezing and excessive heat above 40C (104F)
Will damage wood finishes, plastics and some fabrics.

Do not use

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

KEEP OUT OF REACH OF CHILDREN

Adult supervision recommended for children under 6 years old.

Directions

Dosage: Place enough product on hands to cover all surfaces. Rub hands together until dry.

Administration: Topical

Other information

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

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

DEFENSE AG HAND SANITIZER 
ipa hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79930-7105
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)	0.2 mL  in 100 mL
CURCUMIN (UNII: IT942ZTH98)	1.3 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	yellow (light translucent yellow hint)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79930-7105-1	100 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/30/2020
2	NDC: 79930-7105-2	250 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/30/2020
3	NDC: 79930-7105-3	350 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/30/2020
4	NDC: 79930-7105-4	500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/30/2020
5	NDC: 79930-7105-5	3785 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/25/2020

Labeler - Nexderma (079533940)

Establishment
Name	Address	ID/FEI	Business Operations
Nexderma		079533940	manufacture(79930-7105) , pack(79930-7105) , label(79930-7105)