ANTIMONITE BELLADONNA- antimonite belladonna powder 
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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Antimonite Belladonna

Directions: FOR ORAL USE ONLY.

Take 3-4 times daily. Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age 2: Consult a doctor.

Active Ingredients: Antimonite (Nat. antimony trisulfide) 3X, Atropa belladonna (Nightshade) 4X, Chamomilla (Chamomile) 4X, Bismutum subnitricum (Bismuth) 6X

Inactive Ingredient: Lactose

"prepared using rhythmical processes"

Use: Temporary relief of upset stomach.

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 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 Uriel, East Troy, WI 53120 shopuriel.com

Antimonite Belladonna powder

ANTIMONITE BELLADONNA 
antimonite belladonna powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1037
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U) ANTIMONY TRISULFIDE3 [hp_X]  in 1 g
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA4 [hp_X]  in 1 g
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) MATRICARIA RECUTITA4 [hp_X]  in 1 g
BISMUTH SUBNITRATE (UNII: H19J064BA5) (BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBNITRATE6 [hp_X]  in 1 g
Inactive Ingredients
Ingredient NameStrength
LACTOSE (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-1037-450 g in 1 BOTTLE, GLASS; 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(48951-1037)

Revised: 1/2024
Document Id: 0ec4e273-43f1-f547-e063-6394a90aaff2
Set id: 0bc61339-130a-459b-9c61-2a12b5572347
Version: 5
Effective Time: 20240112
 
Uriel Pharmacy Inc.