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Luffeel

Biologische Heilmittel Heel

LUFFEEL NASAL SPRAY


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

PURPOSE

Galphimia glauca 4X, 12X, 30X 2 ml each.....Relieves allergies, hayfever

Histaminum 12X, 30X, 200X 1 ml each.........Relieves allergic illnesses

Luffa operculata 4X, 12X, 30X 2 ml each......Relieves hayfever nasal symptoms

Sulphur 12X, 30X, 200X 1 ml each...............Relieves nasal congestion, itchy burning eyes

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of the 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

If symptoms persist or worsen, a physician should be consulted. As with any drug, if you are pregnant or nursing a baby, seek the advise of a health care professional before using this product. The use of this dispenser by more than one person may spread infection.

LUFFEEL DOSAGE AND ADMINISTRATION

Adults and children 6 years and over: 1-2 sprays into each nostril 3-5 times daily. Infants and children under 6 years: 1 spray into each nostril 3-4 times daily.

ACTIVE INGREDIENTS

Each 20 ml contains as active ingredients: Galphimia glauca 4X, 12X, 30X 2 ml each, Histaminum 12X, 30X, 200X 1 ml each, Luffa operculata 4X, 12X, 30X 2 ml each, Sulphur 12X, 30X, 200X 1 ml each.

INACTIVE INGREDIENTS

Benzalkonium chloride 0.01%, isotonic saline solution


Luffeel


Luffeel

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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:51885-3100
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:51885-3100-3 1 in 1 CARTON

Marketing Information

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


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Be sure to consult your doctor before taking any medication!
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