Phytolacca decandra

Manufacturer: Boiron | Boiron, Inc.
Effective date: 2023-01-23
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:19:54

Label at a glance#

ProductPhytolacca decandra

Active ingredientPHYTOLACCA AMERICANA ROOT

Label structure10 sections

Contacts and useful links#

PhoneLabel contact1-800-264-7661

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Phytolacca decandra 200CK

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

INDICATIONS & USAGE SECTION

Sore Throat Pain Radiating To The Ears*

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

SPL UNCLASSIFIED SECTION

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.

INACTIVE INGREDIENT SECTION

lactose, sucrose

DOSAGE & ADMINISTRATION SECTION

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.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0220-4207-41	Phytolacca decandra	200 [kp_C] in 1 TUBE	PELLET	200		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0220-4207	PHYTOLACCA DECANDRA (PHYTOLACCA AMERICANA ROOT ) PELLET [BOIRON]	2	Current NDC, Legacy NDC, 1 package rows	20230124_86965d82-e679-8516-e053-2991aa0a83db.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

Phytolacca decandra
PHYTOLACCA AMERICANA ROOT
LACTOSE, UNSPECIFIED FORM
ANHYDROUS LACTOSE
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0220-4207	0220-4207-41

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PHYTOLACCA AMERICANA ROOT	11E6VI8VEG	ACTIB
LACTOSE, UNSPECIFIED FORM	J2B2A4N98G	IACT
SUCROSE	C151H8M554	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Phytolacca decandra	PHYTOLACCA AMERICANA ROOT	Boiron	86965d82-e679-8516-e053-2991aa0a83db	2023-01-23		Exact identifier ndc (package): 0220-4207-41 ndc (product): 0220-4207 ndc11 (package): 00220420741 spl id: f2f5a316-2435-cd5b-e053-2995a90a7362 spl set id: 86965d82-e679-8516-e053-2991aa0a83db

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.