PASSIFLORA CRATAEGUS SPECIAL ORDER- passiflora crataegus 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.

----------

Passiflora Crataegus Special Order

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: Bryophyllum (Life plant) 2X, Crataegus (Hawthorn) 3X, Passiflora (Passionflower) 3X, Salix vitellina (Golden willow) 3X

Inactive Ingredients: Distilled water, 20% Organic cane alcohol

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. 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

PassifloraCrataegusSOLiquid

PASSIFLORA CRATAEGUS SPECIAL ORDER 
passiflora crataegus special order liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-8252
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
KALANCHOE DAIGREMONTIANA LEAF (UNII: L6X13JKL8O) (KALANCHOE DAIGREMONTIANA LEAF - UNII:L6X13JKL8O) KALANCHOE DAIGREMONTIANA LEAF2 [hp_X]  in 1 mL
HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) (HAWTHORN LEAF WITH FLOWER - UNII:6OM09RPY36) HAWTHORN LEAF WITH FLOWER3 [hp_X]  in 1 mL
PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (PASSIFLORA INCARNATA FLOWERING TOP - UNII:CLF5YFS11O) PASSIFLORA INCARNATA FLOWERING TOP3 [hp_X]  in 1 mL
SALIX ALBA FLOWER (UNII: 905Y746BSW) (SALIX ALBA FLOWER - UNII:905Y746BSW) SALIX ALBA FLOWER3 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-8252-360 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/01/200910/09/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/01/200910/09/2020
Labeler - Uriel Pharmacy Inc. (043471163)
Establishment
NameAddressID/FEIBusiness Operations
Uriel Pharmacy Inc.043471163manufacture(48951-8252)

Revised: 12/2020
Document Id: b596066c-d45d-c066-e053-2a95a90ace7e
Set id: 741aabca-aec2-4d60-9809-c0ccc03b1e28
Version: 4
Effective Time: 20201203
 
Uriel Pharmacy Inc.