ARNICA RETINA QUARTZ SPECIAL ORDER- arnica retina quartz 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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Arnica Retina Quartz Special Order

Directions: FOR ORAL USE.

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

Active Ingredients: Antimonite 10X, Retina et chorioidea 10X, Quartz 12X, Arnica e pl. tota 20X, Equisetum ex herba 20X

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 Uriel, East Troy, WI 53120 www.urielpharmacy.com

ArnicaRetinaQuartzSpecialOrderAmpules

ARNICA RETINA QUARTZ SPECIAL ORDER 
arnica retina quartz special order liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1252
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U) ANTIMONY TRISULFIDE10 [hp_X]  in 1 mL
BOS TAURUS EYE (UNII: VTW461N43P) (BOS TAURUS EYE - UNII:VTW461N43P) BOS TAURUS EYE10 [hp_X]  in 1 mL
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE12 [hp_X]  in 1 mL
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA20 [hp_X]  in 1 mL
EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z) EQUISETUM ARVENSE TOP20 [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:48951-1252-110 in 1 BOX09/01/2009
11 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package
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(48951-1252)

Revised: 7/2017
Document Id: 55517295-1285-4930-e054-00144ff8d46c
Set id: 62dc33e1-8cb1-4858-8ef8-194cd6246daa
Version: 2
Effective Time: 20170727
 
Uriel Pharmacy Inc.