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FLUEndz

Herbology International LLC
Herbology International LLC




FULL PRESCRIBING INFORMATION

Uses

  • For relief of symptoms associated with the flu and common cold as per Homeopathic Materia Medica.

Inactive Ingredients:   Ascorbic acid, alcohol, purified water and zinum gluconicum

  • Adults and children 12 years and over:  Spray twice under the tongue every 4-5 hours, up to 5 times a day.  For severe symptoms, dosage may be taken up to 6 times the first day.
  • Children 2 to 12 years:  Spray once under the tongue every 4-5 hours, up to 3 times per day.  For severe symptoms, dosage may be taken up to 4 times the first day.
  • Children under 2 years of age:  Consult a doctor prior to use.

Warnings:

  • Stop use and ask a doctor if symptoms persist for more than 7 days.
  • Do not use if you have an allergy or hypersensitivity to components of the formula.
  • If pregnant or breast feeding ask a health professional before use.
  • Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.
  • No Side Effects
  • Non Drowsy
  • No Interactions with Other Medications



  • Fever
  • Chills
  • Sore Throat
  • Congestion
  • Cough
  • Vomiting
  • Headache
  • Nausea
  • Body Aches
  • Weakness
  • Running Nose
  • Dizziness
FLUEndz

Questions or Comments? 1-877-FLU-1288 Monday through Friday, 9am-5pm or www.FLUEndz.com

Developed, Formulated and Distributed by:
Herbology International
Roseville, California 95661
All rights reserved
U.S. Patents Pending

Manufactured by: Apotheca Inc., Woodbine, IA 51579, 1-800-736-3130

Other Information

  • Store at 20-25 degrees C (68-77 degrees F)
  • Avoid eating 30 minutes before and after taking FLUEndz
  • The letters HPUS imply that these ingredients are officially included in the Homeopathic Pharmacopoeia of the United States

FLUEndz

Asafoetida, Astragalus Menziesii, Illicium Anisatum, Lonicera Zylosteum SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50367-100
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ASAFETIDA ASAFETIDA 3 [hp_X]
ASTRAGALUS NUTTALLII LEAF ASTRAGALUS NUTTALLII LEAF 6 [hp_X]
STAR ANISE STAR ANISE 1 [hp_X]
LONICERA XYLOSTEUM FRUIT LONICERA XYLOSTEUM FRUIT 6 [hp_X]

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50367-100-01 20 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2010-01-15


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Be sure to consult your doctor before taking any medication!
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