Luffeel description, usages, side effects, indications, overdosage, supplying and lots more!

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Luffeel

Heel Inc

Luffeel Nasal Spray


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

PURPOSE

Galphimia glauca 4X, 12X, 30X....................Relieves runny nose and sneezing

Histaminum 12X, 30X, 200X........................Relieves nasal congestion and itching

Luffa operculata 4X, 12X, 30X......................Relieves runny nose and sneezing

Sulphur 12X, 30X, 200X .............................Relieves nasal congestion and itchy watery eyes

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

LUFFEEL INDICATIONS AND USAGE

For the temporary relief of symptoms of hay fever:

  • itchy and watery eyes
  • sneezing
  • runny nose
  • nasal congestion

WARNINGS

Ask a doctor before use if you have asthma. In rare cases bronchospasm may occur in asthmatic patients. Temporary burning, stinging, sneezing, or increased nasal discharge may occur. If pregnant or breast-feeding, ask a healthcare provider before use. Do not use if known sensitivity to Luffeel or any of its ingredients exists. Keep out of reach of children. The use of this dispenser by more than one person may spread infection. If symptoms persist or worsen, a healthcare provider should be consulted.

LUFFEEL DOSAGE AND ADMINISTRATION

Directions                  Standard Dosage                        Initial Dosage















ACTIVE INGREDIENTS

INACTIVE INGREDIENTS

Luffeel

Luffeel

GALPHIMIA GLAUCA FLOWERING TOP and HISTAMINE DIHYDROCHLORIDE and LUFFA OPERCULATA FRUIT and SULFUR SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50114-0150
Route of Administration NASAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
galphimia glauca flowering top GALPHIMIA GLAUCA FLOWERING TOP 4 [hp_X]
HISTAMINE DIHYDROCHLORIDE Histamine 12 [hp_X]
LUFFA OPERCULATA FRUIT LUFFA OPERCULATA FRUIT 4 [hp_X]
SULFUR SULFUR 12 [hp_X]

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
SODIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 20 in 1 BOTTLE, PUMP
2 NDC:50114-0150-9 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-07-05


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