LACHESIS BELLADONNA- lachesis belladonna pellet 
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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Lachesis Belladonna

Directions: FOR ORAL USE ONLY.

Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

Active Ingredients: Mercurialis (Dog's mercury) 3X, Atropa belladonna (Nightshade) 4X, Hepar sulfuris (Sulphurated lime) 6X, Lachesis e veneno (Bushmaster venom) 12X

Inactive Ingredient: Organic sucrose

Use: Promotes healing of wounds.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. 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 Uriel, East Troy, WI 53120 www.urielpharmacy.com

LachesisBelladonnaPellets

LACHESIS BELLADONNA 
lachesis belladonna pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-6014
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MERCURIALIS PERENNIS (UNII: Q35465A1MA) (MERCURIALIS PERENNIS - UNII:Q35465A1MA) MERCURIALIS PERENNIS3 [hp_X]
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA4 [hp_X]
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE6 [hp_X]
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM12 [hp_X]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-6014-21350 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(48951-6014)

Revised: 6/2018
Document Id: 6de5a51a-67ac-31ce-e053-2991aa0afb4d
Set id: 5d8ff4a3-9395-4264-9b18-eae5f499aa59
Version: 3
Effective Time: 20180605
 
Uriel Pharmacy Inc.