ARNICA E PL. TOTA 20X SPECIAL ORDER- arnica e pl. tota 20x 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 e pl. tota 20X 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 Ingredient: Arnica e pl. tota 20X

Inactive Ingredient: Distilled water

Use: Temporary relief of sore muscles.

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 90 DAYS OF OPENING.

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

ArnicaEpl.Tota20XSOLiquid

ARNICA E PL. TOTA 20X SPECIAL ORDER 
arnica e pl. tota 20x special order liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1337
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA20 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-1337-360 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(48951-1337)

Revised: 11/2019
Document Id: 6a0db083-3391-b3ab-e053-2a91aa0a1dd5
Set id: 69cc3c03-4ad8-463f-8582-499f3628fd8c
Version: 3
Effective Time: 20191125
 
Uriel Pharmacy Inc.