Label: SEVERE SINUS RELIEF MIST- oxymetazoline spray liquid
- NDC Code(s): 0363-2305-52
- Packager: Walgreens Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 14, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Purpose
- Uses
- Warnings
- Ask a Doctor before use if you have
-
When using this product
- Do not use more than directed
- do not use for more than three days, Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen.
- temporary discomfort such as burning ,stinging, sneezing or an increase in nasal discharge may occur.
- use of this container by more than one person may spread infection.
- stop use and ask a doctor if
- if pregnant or breast-feeding
- Keep out of the reach of children
-
Directions
- Before using for the first time, remove the protective cap form the tip and prime the pump by depressing pump firmly several times. To spray, hold bottle with thumb at base and nozzle between first and second fingers. Without tilting head, insert nozzle into nostrile. Fully depress rim with a firm and even stroke, and sniff deeply.
- Wipe nozzle clean after use.
- Adults and children 6 to under 12 years of age (with adult supervision):2 or 3 sprays in each nostril not more than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period.
- Children under 6 years of age consult a doctor.
- Other information
- Questions or Comments ? 1-800-222-1087
- Inactive Ingredients
- Principal Panel 0.5 FLOZ Bottle
- Principal display panel -Carton
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INGREDIENTS AND APPEARANCE
SEVERE SINUS RELIEF MIST
oxymetazoline spray liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-2305 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE 50 mg in 100 mL Inactive Ingredients Ingredient Name Strength POLYSORBATE 80 (UNII: 6OZP39ZG8H) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW) SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74) BENZYL ALCOHOL (UNII: LKG8494WBH) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) WATER (UNII: 059QF0KO0R) MENTHOL (UNII: L7T10EIP3A) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) EUCALYPTOL (UNII: RV6J6604TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-2305-52 1 in 1 CARTON 08/30/2018 1 15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 08/30/2018 Labeler - Walgreens Company (008965063)
