CUPRUM STANNUM- cuprum stannum 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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Cuprum Stannum

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: 100gm contains: 94gm Acidum nitricum (Nitric acid) 2X, 40gm Acidum sulfuricum (Sulfuric acid) 2X, 20gm Stannum met. (Metallic tin) 2X, 2gm Cuprum met. (Copper) 3X; Alumen (Potassium aluminum sulfate) 3X

Inactive Ingredients: Distilled water, Silica, Lactose

Use: Temporary relief of digestive upset.

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 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 www.urielpharmacy.com

CuprumStannumLiquid

CUPRUM STANNUM 
cuprum stannum liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-3145
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4) NITRIC ACID2 [hp_X]  in 1 mL
SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF) SULFURIC ACID2 [hp_X]  in 1 mL
TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN2 [hp_X]  in 1 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER3 [hp_X]  in 1 mL
POTASSIUM ALUM (UNII: 1L24V9R23S) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) POTASSIUM ALUM3 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
LACTOSE (UNII: J2B2A4N98G)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-3145-360 mL 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(48951-3145)

Revised: 4/2018
Document Id: 6aae749e-f391-1638-e053-2991aa0a6434
Set id: 2f5f86d5-a405-4bfd-80e3-2e1cf6f64bc2
Version: 4
Effective Time: 20180425
 
Uriel Pharmacy Inc.