Preferred Plus 12 Hour Nasal description, usages, side effects, indications, overdosage, supplying and lots more!

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Preferred Plus 12 Hour Nasal

Kinray
Lee Pharmaceuticals

Drug Facts




FULL PRESCRIBING INFORMATION

Oxymetazoline Hydrochloride, 0.05%

Nasal Decongestant

  • Temporarily relieves nasal decongestion due to:  common cold, hay fever, sinusitis, upper respiratory allergies
  • Shrinks swollen nasal membranes so you can breathe more freely

  • Heart disease
  • High blood pressure
  • Diabetes
  • Thyroid disease
  • Trouble urinating due to an enlarged prostate gland
  • Do not use more than directed
  • Do not use for more than 3 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 symptoms persists.

If pregnant or breast-feeding, ask a health professional before use.

Keep o ut of reach of children.  If swallowed, get medical help or contact a Poison Control Center immediately.

  • Adults and children 6 to under 12 years of age (with adult supervision):  2 or 3 sprays in each nostril not more often than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period.
  • Children under 6 years of age:  ask a doctor
  • To spray, squeeze bottle quickly and firmly.  Do not tilt head backwards while spraying.  Wipe nozzle clean after use
  • Store between 20° - 25° C (68° - 77° F)
  • Retain carton for future reference on full labeling.

Benzalkonium chloride, edetate disodium, glycerin, polyethylene glycol, povidone, propylene glycol, sodium phosphate dibasic, sodium phosphate monobasic, water

Preferred Plus 12 Hour Nasal

Preferred Plus 12 Hour Nasal

Preferred Plus 12 Hour Nasal

Oxymetazoline Hydrochloride SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:61715-047
Route of Administration NASAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OXYMETAZOLINE HYDROCHLORIDE OXYMETAZOLINE 50.0 mg

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
EDETATE DISODIUM ANHYDROUS
GLYCERIN
POLYETHYLENE GLYCOL 3350
povidone
propylene glycol
SODIUM PHOSPHATE, DIBASIC
sodium phosphate, monobasic
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61715-047-01 30 in 1 BOTTLE, SPRAY
2 NDC:61715-047-02 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2008-01-31


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Be sure to consult your doctor before taking any medication!
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