Scorodite Prunus

SCORODITE PRUNUS- scorodite prunus 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.

----------

Scorodite Prunus

Directions: FOR ORAL USE ONLY.

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

Active Ingredients: Camphora (Camphor) 4X, Veratrum (White hellebore) 4X, Prunus spinosa (Blackthorn) 6X, Scorodite (Nat. ferric arsenate) 6X, Hypophysis (Bovine pituitary gland) 8X, Aurum met. (Metallic gold) 10X

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. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditons worsen or persist. If pregnant or nursing consult a doctor before use.

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

ScoroditePrunusAmpules

SCORODITE PRUNUS
scorodite prunus liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-8168
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	4 [hp_X] in 1 mL
VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (VERATRUM ALBUM ROOT - UNII:QNS6W5US1Z)	VERATRUM ALBUM ROOT	4 [hp_X] in 1 mL
SLOE (UNII: 3MLB4858X7) (SLOE - UNII:3MLB4858X7)	SLOE	6 [hp_X] in 1 mL
FERROUS ARSENATE (UNII: 129CO35H12) (FERROUS ARSENATE - UNII:129CO35H12)	FERROUS ARSENATE	6 [hp_X] in 1 mL
BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K) (BOS TAURUS PITUITARY GLAND - UNII:7JM57I419K)	BOS TAURUS PITUITARY GLAND	8 [hp_X] in 1 mL
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	10 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
LACTOSE (UNII: J2B2A4N98G)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:48951-8168-1	10 in 1 BOX	09/01/2009
1		1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/01/2009

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-8168)