Euphrasia Officinalis: Homeopathic Product Information

EUPHRASIA OFFICINALIS- euphrasia stricta pellet
Boiron

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.

Euphrasia officinalis 1M

(**contains 0.443 mg of the active ingredient per pellet)

Abundant And Irritating Eye Discharge*

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen

If pregnant or breast-feeding ask a health professional before use

Keep out of reach of children

Do not use if pellet dispenser seal is broken.
Contains approx 80 pellets.
How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully remove the cap and use it to pour pellets under the tongue.
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
*C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

lactose, sucrose

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

1-800-BOIRON-1 (1-800-264-7661),
BoironUSA.com Info@boiron.com
Distributed by Boiron, Inc. Newtown Square, PA 19073

EUPHRASIA OFFICINALIS euphrasia stricta pellet

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-1997 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUPHRASIA STRICTA (EUPHRASIA STRICTA) EUPHRASIA STRICTA 1 [hp_M] in 1 [hp_M]

Inactive Ingredients Ingredient Name Strength SUCROSE LACTOSE, UNSPECIFIED FORM (ANHYDROUS LACTOSE)

Product Characteristics Color white Score Shape ROUND Size 4mm Flavor Imprint Code Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:0220-1997-41 1 [hp_M] in 1 TUBE None

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/03/1983

Labeler — Boiron (282560473)

Registrant — Boiron, Inc. (014892269)

Establishment
Name	Address	ID/FEI	Operations
Boiron		282560473	manufacture (0220-1997)

Revised: 08/2023 Boiron