NOZIN NASAL SANITIZER- alcohol liquid 
Denison Pharmaceuticals, LLC

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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Nozin Nasal Sanitizer

Active ingredient

Alcohol 62%

Inactive ingredients

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

Purpose

Antiseptic

Use

  • to decrease bacteria on the skin

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 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

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 information

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

label

NOZIN NASAL SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0295-9025
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0295-9025-6212 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/09/2020
Labeler - Denison Pharmaceuticals, LLC (001207208)
Establishment
NameAddressID/FEIBusiness Operations
Denison Pharmaceuticals, LLC001207208manufacture(0295-9025)

Revised: 4/2020
 
Denison Pharmaceuticals, LLC