Nozin Nasal Sanitizer

Manufacturer
Denison Pharmaceuticals, LLC
Effective date
2020-04-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:36:44

Label at a glance#

ProductNozin Nasal Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 62%

INACTIVE INGREDIENT SECTION

Inactive ingredients

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

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Use

  • to decrease bacteria on the skin

WARNINGS SECTION

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

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0295-90250295-9025-62

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a2dec922-6911-ecd1-e053-2a95a90ad099a2dec922-6910-ecd1-e053-2a95a90ad0992020-04-09WarningsExact identifier
spl id: a2dec922-6911-ecd1-e053-2a95a90ad099
spl set id: a2dec922-6910-ecd1-e053-2a95a90ad099

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.