K-Loss by NARTEX LABORATORIOS HOMEOPATICOS SA DE CV / 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, LABORATORIOS HOMEOPATICOS SA DE CV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

K-LOSS- fucus vesiculosus, graphites, phytolacca decandra pellet 
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.

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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

Keep box

as it contains important information.

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 3 pellets orally before each meal
• 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

Sucrose

Questions or comments?

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

K-LOSS 
fucus vesiculosus, graphites, phytolacca decandra pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 34666-031
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
SUCROSE (UNII: C151H8M554)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 34666-031-50	150 in 1 BOTTLE, GLASS; 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 - LABORATORIOS HOMEOPATICOS SA DE CV (589914576)

Establishment
Name	Address	ID/FEI	Business Operations
LABORATORIOS HOMEOPATICOS SA DE CV		589914576	manufacture(34666-031)

Revised: 12/2019

Document Id: 9aa3935d-290f-1b3d-e053-2a95a90a81d6

34390-5

Set id: d644a0ec-677b-4b29-adc9-8734353a3c1e

Version: 3

Effective Time: 20191226

 

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