ARNICA E PL. TOTA 30X- arnica e pl. tota 30x 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 30X

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 (Arnica) 30X

Inactive Ingredients: Distilled water, 20% Organic cane alcohol

"prepared using rhythmical processes"

Use: Temporary relief of headache and 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.

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

Arnica e pl. tota 30X Liquid

ARNICA E PL. TOTA 30X 
arnica e pl. tota 30x liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1367
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA30 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-1367-360 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(48951-1367)

Revised: 12/2023
Document Id: 0c7dc8ac-5119-db15-e063-6294a90a774e
Set id: 0c429f2a-02ff-0850-e063-6394a90ac0e2
Version: 2
Effective Time: 20231214
 
Uriel Pharmacy, Inc.