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FluNada

Flutrends International Corporation

FluNada Cold and Flu Relief - Drug Facts Label


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients: (in each 20 mL)

Eucalyptol 3x HPUS

Eucalyptus globulus 3x HPUS

Gaultheria 3x HPUS

Mentholum 4x HPUS

Sambucus nigra 2x HPUS

Purpose

  • Stuffed up nose, watery nose
  • Sore throat, runny or stuffed nose, headache
  • Aches and/or pains
  • Post nasal drip, runny nose, headache, sore throat
  • Blocked or stuffy nose, cough

The letters HPUS indicate that this ingredient is officially included in the Homeopathic Pharmacopoeia of the United States.

Uses:

For relief of cold and flu-like symptoms such as nasal congestion, runny or blocked nose, post nasal drip, sore throat, cough and headache. For optimal results, use at first sign of cold or flu-like symptoms.

Warnings:

  • Do not use if pump bottle seal is broken.
  • Use of this dispenser by more than one person can spread infection.
  • Ask a doctor before use if you have asthma or known allergies to any product ingredient, or a history of nose bleeds.
  • Consult a healthcare professional if you are pregnant or breast-feeding.
  • Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.
  • Ask a doctor before use in children younger than 4 years of age.
  • Keep out of reach of children.

Directions:

  • Adults and children 4 years and older. Spray 3 times to throat and swallow; also spray once into each nostril, let drip, then swallow.
  • Use up to 4 times daily, up to 5 days.
  • Store at room temperature in a cool, dry place.

Inactive Ingredients:

Citric acid, ethanol, glycerin, poloxamer 407, sodium benzoate, sodium chloride, sorbitol, thymol, water, xylitol.

FOR QUESTIONS / COMMENTS:

call (888) 407-2816

www.flunada.com

Image of 20mL Carton and Label

FluNadaCarton.jpgFluNada FluNadaLabel.jpgFluNada

FluNada

EUCALYPTOL, EUCALYPTUS GLOBULUS WHOLE, MENTHOL, SAMBUCUS NIGRA WHOLE, METHYL SALICYLATE SPRAY, METERED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54705-160
Route of Administration NASAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
EUCALYPTOL EUCALYPTOL 3 [hp_X]
EUCALYPTUS GLOBULUS WHOLE 3 [hp_X]
MENTHOL 4 [hp_X]
SAMBUCUS NIGRA WHOLE SAMBUCUS NIGRA WHOLE 2 [hp_X]
methyl salicylate METHYL SALICYLATE 3 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL
Xylitol
POLOXAMER 407
GLYCERIN
sorbitol
SODIUM CHLORIDE
CITRIC ACID MONOHYDRATE
SODIUM BENZOATE
THYMOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:54705-160-20 20 in 1 BOTTLE, SPRAY
2 NDC:54705-160-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2012-12-18


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