K-Loss by NARTEX LABORATORIOS HOMEOPATICOS SA DE CV

K-Loss by

Drug Labeling and Warnings

K-Loss by is a Homeopathic medication manufactured, distributed, or labeled by NARTEX LABORATORIOS HOMEOPATICOS SA DE CV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

K-LOSS- fucus vesiculosus, graphites, phytolacca decandra tablet 
NARTEX LABORATORIOS HOMEOPATICOS SA DE CV

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

----------

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

Fucus vesiculosus...............Appetite control

Graphites..........................Metabolic control

Phytolacca decandra.......................Obesity

Weight loss aid as per homeopathic materia medica.

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 
fucus vesiculosus, graphites, phytolacca decandra tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 34666-040
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M)	FUCUS VESICULOSUS	4 [hp_X]
GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O)	GRAPHITE	4 [hp_X]
PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG)	PHYTOLACCA AMERICANA ROOT	4 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
GELATIN (UNII: 2G86QN327L)
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
STARCH, POTATO (UNII: 8I089SAH3T)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	white (Nartex Logo)	Score	no score
Shape	ROUND (none)	Size	10mm
Flavor		Imprint Code	none
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 34666-040-60	60 in 1 BLISTER PACK; Type 0: Not a Combination Product	07/25/2011	12/26/2019
2	NDC: 34666-040-06	60 in 1 BLISTER PACK; Type 0: Not a Combination Product	07/25/2011	12/26/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		07/25/2011	12/26/2019

Labeler - NARTEX LABORATORIOS HOMEOPATICOS SA DE CV (589914576)

Registrant - NARTEX LABORATORIOS HOMEOPATICOS SA DE CV (589914576)

Establishment
Name	Address	ID/FEI	Business Operations
NARTEX LABORATORIOS HOMEOPATICOS SA DE CV		589914576	manufacture(34666-040)

Revised: 12/2019

Document Id: 9aa3a72a-e14b-1b4b-e053-2a95a90adfd4

34390-5

Set id: d468e71a-aa48-4ca2-a96f-33ceffa53dc8

Version: 6

Effective Time: 20191226

 

N