SINUFRIN PLUS NEILMED- oxymetazoline hydrochloride spray 
NeilMed Pharmaceuticals, Inc.

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 Facts

Active Ingredients

0.05% Oxymetazoline Hydrochloride


Directions for Dosing

    * Adults and children 6 to 12 years of age (with adult supervision): Per dose, 2 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: consult a doctor


Temporarily relieves nasal congestion due to common cold, sinus infections, hay fever, upper respiratory allergies.

Other Information

Store between 20 to 40 °C (68 to 104 °F)
Retain carton for future reference on full labeling


KEEP OUT OF REACH OF CHILDREN. If Swallowed,get medical help or contact a Poison Control Center right away.

Do not use this product for more than 3 consecutive days.

Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen. If symptoms persist, consult a doctor.

Other Information


Stop use and ask a doctor if symptoms of nasal congestion persist after 3 days.

Adult males with prostate disease, do not use this product.


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


This product may cause temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge.
The use of this container by more than one person may spread infection.

Inactive ingredients

Propylene glycol, glycerin, sodium chloride, hyaluronic acid, aloe vera, allantoin, sodium bicarbonate USP, benzalkonium chloride, edetate disodium, purified water

Principle Display

Imag of BottleImage of bottle

Box Label

Box label


temporarily relieves nasal congestion due to:

common cold


hay fever

upper respiratory allergies

oxymetazoline hydrochloride spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:13709-232
Route of Administration NASAL DEA Schedule CII    
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Oxymetazoline Hydrochloride (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) Oxymetazoline Hydrochloride 7.5 mg  in 15 mL
Inactive Ingredients
Ingredient Name Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Sodium Chloride (UNII: 451W47IQ8X)  
water (UNII: 059QF0KO0R)  
Sodium Bicarbonate (UNII: 8MDF5V39QO)  
Glycerin (UNII: PDC6A3C0OX)  
Aloe (UNII: V5VD430YW9)  
Allantoin (UNII: 344S277G0Z)  
Hydrochloric Acid (UNII: QTT17582CB)  
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:13709-232-06 15 mL in 1 BOTTLE
2 NDC:13709-232-05 15 mL in 1 BOX
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part341 07/15/2012
Labeler - NeilMed Pharmaceuticals, Inc. (783557783)
Name Address ID/FEI Business Operations
NeilMed Pharmaceuticals, Inc. 783557783 manufacture(13709-232)

Revised: 9/2012
Document Id: c243e7d4-0748-468b-8e25-b914adafdf83
Set id: 99afe6a6-1350-49c6-9347-b7e531e35925
Version: 2
Effective Time: 20120915
NeilMed Pharmaceuticals, Inc.