NICOTIANA PULSATILLA SPECIAL ORDER- nicotiana pulsatilla special order 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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Nicotiana Pulsatilla Special Order

Directions: FOR ORAL USE.

Take the contents of one ampule under the tounge and hold for 30 seconds, then swallow.

Active Ingredients: Berberis e fruct. 3X, Pulsatilla e flor. 4X, Nicotiana e fol. 8X

Inactive Ingredients: Water, Salt

Use: Temporary relief of headache.

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.

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

NicotianaPulsatillaSOAmpules

NICOTIANA PULSATILLA SPECIAL ORDER 
nicotiana pulsatilla special order liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-7075
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 3 [hp_X]  in 1 mL
PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 4 [hp_X]  in 1 mL
TOBACCO LEAF (UNII: 6YR2608RSU) (TOBACCO LEAF - UNII:6YR2608RSU) TOBACCO LEAF 8 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:48951-7075-1 10 in 1 BOX 09/01/2009
1 1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 09/01/2009
Labeler - Uriel Pharmacy Inc. (043471163)
Establishment
Name Address ID/FEI Business Operations
Uriel Pharmacy Inc. 043471163 manufacture(48951-7075)

Revised: 8/2017
Document Id: 55dc93ad-c54d-234f-e054-00144ff8d46c
Set id: 19392541-4b12-454f-8fbb-ff169f1b790c
Version: 2
Effective Time: 20170803
 
Uriel Pharmacy Inc.