KENZAPUR - glonoinum, lachesis mutus, natrum muriaticum, natrum sulphuricum, thuja occidentalis liquid 
OHM PHARMA INC.

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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KENZAPUR


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

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


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


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 bottle label

Kenzapur box

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KENZAPUR  
glonoinum, lachesis mutus, natrum muriaticum, natrum sulphuricum, thuja occidentalis liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66096-688
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NITROGLYCERIN (UNII: G59M7S0WS3) (NITROGLYCERIN - UNII:G59M7S0WS3) NITROGLYCERIN6 [hp_X]  in 1 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM12 [hp_X]  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE6 [hp_X]  in 1 mL
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE6 [hp_X]  in 1 mL
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG9 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66096-688-172 in 1 CARTON07/01/201312/19/2017
150 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/01/201312/19/2017
Labeler - OHM PHARMA INC. (030572478)
Registrant - OHM PHARMA INC. (030572478)
Establishment
NameAddressID/FEIBusiness Operations
OHM PHARMA INC.030572478manufacture(66096-688)

Revised: 12/2017
Document Id: b2c46e96-3f41-4fa5-84c2-5c05b9527246
Set id: d1545ff9-a0d0-4af3-87ef-1466cffec0d2
Version: 2
Effective Time: 20171219
 
OHM PHARMA INC.