Sabadilla: Homeopathic Product Information

SABADILLA- schoenocaulon officinale seed 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.

Sabadilla 6X

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

Itchy throat due to hay fever*

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

label
(click image for full-size original)

SABADILLA
schoenocaulon officinale seed pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-4502
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SCHOENOCAULON OFFICINALE SEED (SCHOENOCAULON OFFICINALE SEED) SCHOENOCAULON OFFICINALE SEED 6 [hp_X]
Inactive Ingredients
Ingredient Name Strength
SUCROSE
LACTOSE
Product Characteristics
Color white Score
Shape ROUND Size 4mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0220-4502-41 80 PELLET 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 (0220-4502)

Revised: 04/2019 Boiron

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