ARGENTUM VISCUM- argentum viscum 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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Argentum Visucum

Directions: FOR ORAL USE.

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

Active Ingredients: Silver chloride 6X, Viscum Mali (Apple tree mistletoe) 6X, Corpus vitreum (Bovine vitreous body of the eye) 8X, Lens cristallina (Bovine crystalline lens of the eye) 12X

Inactive Ingredients: Water, Salt, Sodium bicarbonate, Rose oil, Lactose

Use:Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN.

REFRIGERATE AFTER OPENING. USE WITHIN 30 DAYS OF OPENING.

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. Do not use if safety seal is broken or missing.

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

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ARGENTUM VISCUM 
argentum viscum liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1102
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SILVER CHLORIDE (UNII: MWB0804EO7) (SILVER CATION - UNII:57N7B0K90A) SILVER CHLORIDE6 [hp_X]  in 1 mL
VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (VISCUM ALBUM FRUITING TOP - UNII:BK9092J5MP) VISCUM ALBUM FRUITING TOP6 [hp_X]  in 1 mL
BOS TAURUS EYE (UNII: VTW461N43P) (BOS TAURUS EYE - UNII:VTW461N43P) BOS TAURUS EYE8 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
ROSE OIL (UNII: WUB68Y35M7)  
LACTOSE (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-1102-11 in 1 BAG09/01/2009
17 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
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(48951-1102)

Revised: 4/2018
Document Id: 69fd113a-5bef-14ae-e053-2991aa0a2254
Set id: 443fe934-f658-41b3-ad7c-f4ae765e0299
Version: 4
Effective Time: 20180416
 
Uriel Pharmacy Inc.