Sevene USA (as PLD) - Phytolacca Decandra 30c (76472-1157)

Manufacturer: SEVENE USA
Effective date: 2026-10-29
Label type: HUMAN OTC DRUG LABEL
Version: 22
Source: daily-update
Hydrated at: 2026-11-03 06:04:35

Label at a glance#

ProductPhytolacca Decandra

Active ingredientPHYTOLACCA AMERICANA ROOT

Label structure13 sections

Dosage and administration

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

Contacts and useful links#

Websitewww.ollois.com

WWW.OLLOIS.COM

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

HOMEOPATHIC DILUTION OF HPUS Phytolacca Decandra 30c.

TRADITIONALLY USE FOR:

OTC - PURPOSE SECTION

Sore throat with pain swallowing*

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

USE:

INDICATIONS & USAGE SECTION

Condition listed above or as directed by a physician.

WARNINGS:

WARNINGS SECTION

Stop use and ask a physician 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.

OTHER INFORMATION:

OTHER SAFETY INFORMATION

Store at room temperature.

OTC - DO NOT USE SECTION

Do not use if pellet-dispenser seal is broken.

INACTIVE INGREDIENT:

INACTIVE INGREDIENT SECTION

Sucrose.

QUESTIONS?

OTC - QUESTIONS SECTION

INFO@OLLOIS.COM * WWW.OLLOIS.COM * MADE IN FRANCE. NOT REVIEWED BY THE FDA AND NOT GUARANTEED TO BE EFFECTIVE. THIS HOMEOPATHIS DILUTION MAY NOT BE SUSEPTIBLE TO SCIENTIFIC MEASUREMENT.

USE:

RECENT MAJOR CHANGES SECTION

Condition listed above or as directed by a physician.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

phytolacca 30c p1phytolacca 30c p2phytolacca 30c p3

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0855717003468	GTIN-13: 0855717003468 EAN-13: 0855717003468 GTIN-12: 855717003468 UPC-A: 855717003468 GTIN storage (14 digits): 00855717003468	PHYTOLACCA_30c_P1.jpg

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
PHYTOLACCA AMERICANA ROOT	ACTIVE INGREDIENT	11E6VI8VEG	5
PHYTOLACCA AMERICANA ROOT	ACTIVE MOIETY	11E6VI8VEG	5
sucrose	INACTIVE INGREDIENT	C151H8M554	5

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Phytolacca Decandra
PHYTOLACCA AMERICANA ROOT
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76472-1157	76472-1157-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PHYTOLACCA AMERICANA ROOT	11E6VI8VEG	ACTIB
SUCROSE	C151H8M554	IACT

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
21	2024-01-30	full-release	2026-06-01 02:25:57

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
sucrose	SUCROSE	C151H8M554	TABLET / SUBLINGUAL	109 mg		Exact identifier — unii+route 2 equally ranked IID candidates
sucrose	SUCROSE	C151H8M554	TABLET / SUBLINGUAL	109 mg		Exact identifier — unii+route 2 equally ranked IID candidates

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
10313758-ce8f-96ab-e063-6294a90af4f4			f749220f-2ad5-4ea4-9d3b-87f8ae4c1ec8	2024-01-30	Warnings	Exact identifier spl set id: f749220f-2ad5-4ea4-9d3b-87f8ae4c1ec8

Reported adverse events (FAERS/openFDA)#

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