Label: NOZIN NASAL SANITIZER- alcohol liquid
- NDC Code(s): 0295-9025-62
- Packager: Denison Pharmaceuticals, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated April 9, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NOZIN NASAL SANITIZER
alcohol liquidProduct 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)