K-Loss description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

K-Loss

NARTEX LABORATORIOS HOMEOPATICOS SA DE CV
NARTEX LABORATORIOS HOMEOPATICOS SA DE CV




FULL PRESCRIBING INFORMATION

Active ingredient

Fucus vesiculosus 4x, Graphites 4x, Phytolacca decandra 4x

Purpose





Uses



Do not use if you have an allergy or hypersensitivity to the components of the formula


Ask a doctor before use if you are

  • under a doctor's care for any serious condition
  • taking any other drug

Stop use and ask a doctor if

  • symptoms persist, worsen, or if new symptoms occur
  • rash develops

If pregnant or breast feeding, consult 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.

Directions

  • adults take 1 tablet orally before each meal for up to 90 days
  • dissolve slowly in mouth
  • children under 12 years of age, consult your physician
  • this treatment requires following a low calorie, well balanced diet and supervised daily exercise in order to achieve optimal results

store in a cool and dry place

Gelatin, lactose, magnesium stearate, potato starch, talc

Questions or comments?

informacion@nartexlabs.com or call 1-800-839-0916 between 9am and 5pm CST

K-Loss

K-Loss

Fucus vesiculosus, Graphites, Phytolacca decandra TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:34666-040
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
FUCUS VESICULOSUS FUCUS VESICULOSUS 4 [hp_X]
Graphite GRAPHITE 4 [hp_X]
PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT 4 [hp_X]

Inactive Ingredients

Ingredient Name Strength
GELATIN
LACTOSE
MAGNESIUM STEARATE
STARCH, POTATO
talc

Product Characteristics

Color Size Imprint Code Shape
white (Nartex Logo) 10 mm none ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:34666-040-60 60 in 1 BLISTER PACK
2 NDC:34666-040-06 60 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-07-25


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.