NOZIN NASAL SANITIZER (ANTISEPTIC)- alcohol liquid

Nozin Nasal Sanitizer (Antiseptic) by

Drug Labeling and Warnings

Nozin Nasal Sanitizer (Antiseptic) by is a Otc medication manufactured, distributed, or labeled by Global Life Technologies Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Alcohol 62%

Purpose

Antiseptic

Use

• to decrease bacteria on the nasal vestibule skin

Warnings

For external use only

• Flammable. Keep away from fire or flame.

Do not use

• in the eyes
• on mucous membranes
• if you have history of nasal bleeding or irritation
• if you have allergies to any of the ingredients

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours

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

Directions

• wipe nostrils with tissue
• shake ampule well for 5 seconds
• remove ampule, flip and reinsert into sleeve to expose swab tip. Avoid touching swab tip.
• at dot on sleeve, squeeze firmly to crack inner ampule.
• point swab tip down, squeeze sleeve repeatedly to saturate swab tip
• Application steps: 1. Insert swab tip into RIGHT nostril. Do not go deeper than tip of swab. 2. With moderate pressure, swab around nostril eight (8) times clockwise. Cover all surfaces including inside tip of nostril. 3. squeeze to resaturate swab tip 4. insert ampule into RIGHT nostril again and swab eight (8) times counterclockwise 5. repeat steps 1, 2, 3, 4 in LEFT nostril 6. discard used ampule
• repeat all directions with second ampule, but skip tissue step.

Other information

• store in a cool, dry place between 15°C - 29°C (59°F - 84°F)

Inactive ingredients

jojoba, water, orange oil, lauric acid, benzalkonium chloride, vitamin E

Questions?

Call: 1-877-669-4648 Online: nozin.com

Principal Display Panel – 0.6 mL Carton Label

Nozin®

NASAL SANITIZER®

NOZASEPTIN® FORMULA ADVANCED ANTISEPTIC

KILLS 99.99% OF GERMS

MOISTURIZING FORMULA

HELPS REDUCE RISK OF INFECTION

Push in
to open

Pull Out Shelf

To open, push in tab above.
Pull out along perforation.

RECOMMENDED BY HEALTH PROFFESSIONALS

250 single use ampules
0.020 fl oz (0.6 mL) each
5.07 fl oz (150 mL) total

250 POPSWAB®
SINGLE USE AMPULES

Principal Display Panel – 0.6 mL Carton Label

Nozin®

NASAL SANITIZER®

ANTISEPTIC 0.6 ml

ONE POPSWAB®

SINGLE USE AMPULE

Principal Display Panel – 0.6 mL Carton Label

Nozin®

NASAL SANITIZER®

NOZASEPTIN® FORMULA ADVANCED ANTISEPTIC

KILLS 99.99% OF GERMS

HELPS REDUCE RISK OF INFECTION

FOR PATIENTS
Ampules individually
packed and barcoded

Push in
to open

Pull Out Shelf

To open, push in tab above.
Pull out along perforation.

Popswab® ampules
packed and barcoded

200 single use ampules
0.020 fl oz (0.6 mL) each
4.06 fl oz (120 mL) total

Principal Display Panel – 0.6 mL Carton Label

Nozin®

NASAL SANITIZER®

NOZASEPTIN® FORMULA ADVANCED ANTISEPTIC

PATIENT PREOPERATIVE
NASAL VESTIBULE SKIN ANTISEPTIC
MOISTURIZING FORMULA

HELPS REDUCE RISK OF INFECTION

0.04 fl oz (1.2 mL)

2 Popswab® single use ampules

Principal Display Panel – 12 mL Carton Label

Nozin®

NASAL SANITIZER®

NOZASEPTIN® FORMULA ADVANCED ANTISEPTIC

KILLS 99.99% OF GERMS

MOISTURIZING FORMULA

HELPS REDUCE RISK OF INFECTION

0.406 fl oz (12 mL)

20 COTTON SWABS

INCLUDED TO START

INGREDIENTS AND APPEARANCE

NOZIN NASAL SANITIZER (ANTISEPTIC) 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82539-211
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
jojoba oil (UNII: 724GKU717M)
water (UNII: 059QF0KO0R)
orange oil (UNII: AKN3KSD11B)
lauric acid (UNII: 1160N9NU9U)
benzalkonium chloride (UNII: F5UM2KM3W7)
.alpha.-tocopherol acetate (UNII: 9E8X80D2L0)

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82539-211-10	250 in 1 CASE	01/01/2017
1		1 in 1 BLISTER PACK
1		0.6 mL in 1 AMPULE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 82539-211-12	2 in 1 CASE	01/01/2019
2		200 in 1 BOX
2		1 in 1 BLISTER PACK
2		0.6 mL in 1 AMPULE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3	NDC: 82539-211-02	2 in 1 CASE	01/01/2006
3		250 in 1 BOX
3		0.6 mL in 1 AMPULE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
4	NDC: 82539-211-11	100 in 1 CASE	01/01/2019
4		2 in 1 BLISTER PACK
4		0.6 mL in 1 AMPULE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
5	NDC: 82539-211-62	12 in 1 CASE	06/01/2014
5		1 in 1 BOX
5		12 mL in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/01/2006

Labeler - Global Life Technologies Corp. (601645513)