PLATINUM CICHORIUM- platinum cichorium liquid 
Uriel Pharmacy 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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Platinum Cichorium

Directions: FOR ORAL USE.

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

Active Ingredients: Cichorium (Wild chicory) 3X, Oxalis (Wood sorrel) 3X, Rosmarinus (Rosemary) 3X, Carbo Betulae (Birch wood charcoal) 6X, Pancreas (Bovine pancreas) 6X, Platinum chloratum (Hexachlorophatinic acid) 6X

Inactive Ingredients: Water, Salt, Lactose

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. Contains traces of lactose. If pregnant or nursing, consult a doctor before use.

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com

PlatinumCichoriumAmpules

PLATINUM CICHORIUM 
platinum cichorium liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-8042
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CICHORIUM INTYBUS WHOLE (UNII: 1KE45XD28S) (CICHORIUM INTYBUS WHOLE - UNII:1KE45XD28S) CICHORIUM INTYBUS WHOLE3 [hp_X]  in 1 mL
OXALIS ACETOSELLA LEAF (UNII: U1W3U02EW0) (OXALIS ACETOSELLA LEAF - UNII:U1W3U02EW0) OXALIS ACETOSELLA LEAF3 [hp_X]  in 1 mL
ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79) (ROSMARINUS OFFICINALIS FLOWERING TOP - UNII:8JM482TI79) ROSMARINUS OFFICINALIS FLOWERING TOP3 [hp_X]  in 1 mL
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL6 [hp_X]  in 1 mL
SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (SUS SCROFA PANCREAS - UNII:9Y3J3362RY) SUS SCROFA PANCREAS6 [hp_X]  in 1 mL
PLATINUM (UNII: 49DFR088MY) (PLATINUM - UNII:49DFR088MY) PLATINUM6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
LACTOSE (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-8042-110 in 1 BOX09/01/2009
11 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/01/2009
Labeler - Uriel Pharmacy Inc. (043471163)
Establishment
NameAddressID/FEIBusiness Operations
Uriel Pharmacy Inc.043471163manufacture(48951-8042)

Revised: 8/2017
Document Id: 55df46f4-c00f-2896-e054-00144ff8d46c
Set id: 195a8f18-870e-4168-8784-16f9257b1f73
Version: 2
Effective Time: 20170803
 
Uriel Pharmacy Inc.