ARGENTUM BRYOPHYLLUM- argentum bryophyllum 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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Argentum Bryophyllum

Directions: FOR ORAL USE.

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

Active Ingredients: Bryophyllum (Life plant) 6X, Argentum metallicum (Silver) 10X

Inactive Ingredients: Water, Salt

"prepared using rhythmical processes"

Use: Temporary relief of sleeplessness.

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 Uriel, East Troy, WI 53120 shopuriel.com

Argentum Bryophyllum Ampule

ARGENTUM BRYOPHYLLUM 
argentum bryophyllum liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1369
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
KALANCHOE DAIGREMONTIANA LEAF (UNII: L6X13JKL8O) (KALANCHOE DAIGREMONTIANA LEAF - UNII:L6X13JKL8O) KALANCHOE DAIGREMONTIANA LEAF6 [hp_X]  in 1 mL
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER10 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-1369-110 in 1 BOX09/01/2009
11 mL in 1 AMPULE; Type 0: Not a Combination Product
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(48951-1369)

Revised: 1/2024
Document Id: 0f4f81ea-e264-e248-e063-6294a90a21eb
Set id: 0f4f81dc-f470-ad0e-e063-6294a90ad368
Version: 1
Effective Time: 20240119
 
Uriel Pharmacy Inc.