KENZAPUR description, usages, side effects, indications, overdosage, supplying and lots more!

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KENZAPUR

OHM PHARMA INC.
OHM PHARMA INC.

KENZAPUR




FULL PRESCRIBING INFORMATION

Active ingredient


Active ingredients (HPUS*): Purpose:
Glonoinum 6X, Lachesis mutus 12X  ..............................................................................................
Relieves blood stasis and poor circulation
Natrum muriaticum 6X, Natrum sulphuricum 6X, Thuja Occidentalis 9X  ........................................
Relieves sodium and water retention in tissues

Active ingredient

* The letters "HPUS" indicate that these ingredients are officially monographed in the Homeopathic Pharmacopoeia of the United States.


Uses

Use: Temporarily relieves the appearance of cellulite.


Warnings:

Do not use if safety seal is broken. If pregnant or breast-feeding ask a health care practitioner before use. Keep out of the reach of children. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

Keep out of the reach of children.


Directions:

  • Adults and children above 12 years: 20 drops orally, 4 times per day (before each meal at bedtime)
  • Wait 30 seconds before swallowing
  • Do not mix with any other liquid
  • Not for use by children
  • May be used consecutively for up to one year following which a three-month interval is suggested

Other information:

Store at room temperature and away from sunlight.


Inactive ingredients: Ethanol Alcohol 30%, Purified Water.


Questions or comments?  www.kenzayu.com


Purpose

CELLULITE TREATMENT



KENZAPUR
ANTITOXIN PURIFYING PEARLS

HOMEOPATHIC MEDICINE

1.72 FL OZ (50 ml)
Alcohol 30%

KENZAYU
kenzayu.com

Made in the USA

Distributed by:
Kenzayu Inc.
Kelowna, B.C.
V1W 1V3

KENZAPUR

KENZAPUR

KENZAPUR KENZAPUR

KENZAPUR

Glonoinum, Lachesis mutus, Natrum muriaticum, Natrum sulphuricum, Thuja occidentalis LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:66096-688
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
nitroglycerin NITROGLYCERIN 6 [hp_X]
LACHESIS MUTA VENOM LACHESIS MUTA VENOM 12 [hp_X]
SODIUM CHLORIDE 6 [hp_X]
SODIUM SULFATE SODIUM CATION 6 [hp_X]
THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG 9 [hp_X]

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 50 in 1 BOTTLE, DROPPER
2 NDC:66096-688-17 2 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-07-01


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Be sure to consult your doctor before taking any medication!
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