Label: NASOXINSPRAY- sodium chloride spray spray
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Contains inactivated NDC Code(s)
NDC Code(s): 70508-1601-1 - Packager: FRIANA LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 19, 2016
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PRINCIPAL DISPLAY PANEL
Do not use if seal is broken or missing.
The use of this dispenser by more than one person may spread infection.
If pregnant or breast-feeding, or when using on children younger than 4 years of age, consult a health professional. -
INGREDIENTS AND APPEARANCE
NASOXINSPRAY
sodium chloride spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70508-1601 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 1.2 mg in 10 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70508-1601-1 15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/04/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 04/04/2016 Labeler - FRIANA LLC (079770345) Registrant - FRIANA LLC (079770345) Establishment Name Address ID/FEI Business Operations FRIANA LLC 079770345 manufacture(70508-1601)