PULSATILLA TORMENTILLA- pulsatilla tormentilla 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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Pulsatilla Tormentilla

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: Hepar (Bovine liver) 4X, Magnesium hydroxydatum (Magnesium hydroxide) 4X, Pulsatilla (Pasqueflower) 12X, Tormentilla (Bloodwort) 30X

Inactive Ingredients: Distilled water, Propolis

Use: Temporarily relieves symptoms of premenstrual syndrome (PMS).

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.

REFRIGERATE AFTER OPENING.
BEST WHEN USED WITHIN 30 DAYS OF OPENING.

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

PulsatillaTormentillaLiquid

PULSATILLA TORMENTILLA 
pulsatilla tormentilla liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-8099
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAMMAL LIVER (UNII: D0846624BI) (MAMMAL LIVER - UNII:D0846624BI) MAMMAL LIVER4 [hp_X]  in 1 mL
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE4 [hp_X]  in 1 mL
PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS12 [hp_X]  in 1 mL
POTENTILLA ERECTA ROOT (UNII: BI896CKT6B) (POTENTILLA ERECTA ROOT - UNII:BI896CKT6B) POTENTILLA ERECTA ROOT30 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-8099-360 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(48951-8099)

Revised: 4/2018
Document Id: 6b1422ef-3da0-6227-e053-2a91aa0ac046
Set id: e4c5306d-43c5-4c2b-8008-95db8fe0d1df
Version: 4
Effective Time: 20180430
 
Uriel Pharmacy Inc.