Nasal Allergy Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Nasal Allergy Relief

Similasan Corporation

Similasan Nasal Allergy Relief


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients..........Purpose




Uses:


  • allergies accompanied by runny nose, itching and/or burning of the nose, watery eyes, sneezing and swollen mucous membranes (congestion)
  • acute and chronic allergic rhinitis
  • post nasal drip caused by allergies
  • sinus pressure caused by allergies

Warnings:

  • Initial exacerbation of symptoms may occur.
  • Use only if bottle seal is intact.
  • Replace cap tightly after every use.
  • To avoid contamination, do not touch the tip of the container to any surface.
  • Discard open bottle after 6 months.
  • The use of this container by more than one person may spread infection

Ask a doctor before use if you:

  • are susceptible to nose bleeds
  • are prone to ear, nose, or throat sensitivity

Stop use and ask a doctor if:

  • symptoms persist beyond 7 days or if they worsen
If pregnant or breast feeding,
Keep out of reach of children.

Directions:


  • remove tamper-evident palstic seal from bottle
  • lift cap off bottle
  • spray 1-3 times into each nostril
  • use as needed
  • replace cap after use

Other information:



Questions?

1-800-240-9780.www.SimilasanUSA.com




Nasal Allergy Relief

Nasal Allergy Relief

Cardiospermum 6X, Galphimia glauca 6X, Luffa operculata 6X, Sabadilla 6X SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59262-241
Route of Administration NASAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARDIOSPERMUM HALICACABUM FLOWERING TOP CARDIOSPERMUM HALICACABUM FLOWERING TOP 6 [hp_X]
galphimia glauca flowering top GALPHIMIA GLAUCA FLOWERING TOP 6 [hp_X]
LUFFA OPERCULATA FRUIT LUFFA OPERCULATA FRUIT 6 [hp_X]
SCHOENOCAULON OFFICINALE SEED SCHOENOCAULON OFFICINALE SEED 6 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
SODIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59262-241-20 20 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2010-05-15


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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