AURUM STIBIUM HYOSCYAMUS- aurum stibium hyoscyamus 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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Aurum Stibium Hyoscyamus

Directions: FOR ORAL USE ONLY.

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

Active Ingredients: Onopordon (Cotton thistle) 3X, Primula (Cowslip) 3X, Hyoscyamus (Henbane) 4X, Stibium metallicum (Antimony) 8X, Aurum metallicum (Metallic gold) 10X

Inactive Ingredients: Distilled water, Organic cane alcohol

"prepared using rhythmical processes"

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. If pregnant or nursing consult a doctor before use. Do not use if safety seal is broken or missing.

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
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Aurum Stibium hyoscyamus Liquid

AURUM STIBIUM HYOSCYAMUS 
aurum stibium hyoscyamus liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1206
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ONOPORDUM ACANTHIUM FLOWER (UNII: AP97AUF88E) (ONOPORDUM ACANTHIUM FLOWER - UNII:AP97AUF88E) ONOPORDUM ACANTHIUM FLOWER3 [hp_X]
PRIMULA VERIS FLOWER (UNII: W5BET37294) (PRIMULA VERIS FLOWER - UNII:W5BET37294) PRIMULA VERIS FLOWER3 [hp_X]
HYOSCYAMUS NIGER LEAF (UNII: 32IT7G8BAW) (HYOSCYAMUS NIGER LEAF - UNII:32IT7G8BAW) HYOSCYAMUS NIGER LEAF4 [hp_X]
ANTIMONY (UNII: 9IT35J3UV3) (ANTIMONY - UNII:9IT35J3UV3) ANTIMONY8 [hp_X]
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD10 [hp_X]
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SUCROSE (UNII: C151H8M554)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-1206-360 in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/01/2009
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(48951-1206)

Revised: 1/2024
Document Id: 0ec588da-7ccf-6f9d-e063-6294a90a4f8b
Set id: 29ca80e6-3797-4ca2-a9cc-ea384b38ba5b
Version: 6
Effective Time: 20240112
 
URIEL PHARMACY INC.