NOZIN NASAL SANITIZER- alcohol liquid

Nozin Nasal Sanitizer by

Drug Labeling and Warnings

Nozin Nasal Sanitizer by is a Otc medication manufactured, distributed, or labeled by Denison Pharmaceuticals, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Alcohol 62%

INACTIVE INGREDIENT

Inactive ingredients

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

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Use

• to decrease bacteria on the skin

WARNINGS

Warnings

For externel use only

Flammable. Keep away from fire or flame.

Do not use

• as nose spray
• in eyes
• on mucous membranes
• if you have a history of nasal bleeding or irritation
• if you have allergies to any of the ingredients
• more than four times a day

STOP USE

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

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.

DOSAGE & ADMINISTRATION

Directions

adults and children over 12 years of age

• shake bottle very well and remove cap
• apply 2 to 4 drops of solution to the cotton swab
• gently apply wettled cotton to skin inside the rim of one nostril. Swab around nostril rim 6x in each direction. Reapply 2 to 4 drops of solution to cotton swab. Swab around other nostril rim 6x in each direction. Caution: Do not extend the swab into nose beyond swab tip (about 1 cm or 3/8"). Apply to skin only. Swab stem should never enter the nose. Discard swab. Secure cap on bottle.

• children under 12 years of age: should be supervised in use
• children under 2 years of age: ask a doctor

OTHER SAFETY INFORMATION

Other information

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NOZIN NASAL SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0295-9025
Route of Administration	TOPICAL

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
ORANGE OIL (UNII: AKN3KSD11B)
LAURIC ACID (UNII: 1160N9NU9U)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
WATER (UNII: 059QF0KO0R)
SIMMONDSIA CHINENSIS WHOLE (UNII: DFM16KFA82)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0295-9025-62	12 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/09/2020

Labeler - Denison Pharmaceuticals, LLC (001207208)

Establishment
Name	Address	ID/FEI	Business Operations
Denison Pharmaceuticals, LLC		001207208	manufacture(0295-9025)