FDA.reportPublic FDA data

Lycopodium Clavatum

Manufacturer
SEVENE USA
Effective date
2025-02-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:32:01

Label at a glance#

ProductLycopodium Clavatum 200ck
Active ingredientLYCOPODIUM CLAVATUM SPORE
Label structure12 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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

HOMEOPATHIC DILUTION OF HPUS LYCOPODIUM CLAVATUM SPORE 200ck **C,K, CK, AND X ARE HOMEOPATHIC DILUTIONS.

TRADITIONALLY USED FOR

OTC - PURPOSE SECTION

Stinging edemas from stings or allergies, relieved by cold*

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 HOMEOPATHIC DILUTION MAY NOT BE SUSCEPTIBLE TO SCIENTIFIC MEASUREMENT.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Page 1Page 1Page 2Page 2Page 3Page 3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76472-3024-12025-02-11C16284748780-12cef2736-ae5d-d83d-e063-dadaa90ab31fSevene USA (as PLD) - Lycopodium Clavatum 200ck (76472-3024)
76472-3024-12025-01-30C16284748780-12cef2736-ae5d-d83d-e063-dadaa90ab31fSevene USA (as PLD) - Lycopodium Clavatum 200ck (76472-3024)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-3024-1Lycopodium Clavatum200ck80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-3024LYCOPODIUM CLAVATUM 200CK (LYCOPODIUM CLAVATUM) PELLET [SEVENE USA]4Current NDC, Legacy NDC, 1 package rows20250213_cf85a896-a004-5b11-e053-2995a90a4df1.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76472-302476472-3024-1

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
NameUNIIKind
SUCROSEC151H8M554IACT
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lycopodium Clavatum 200ckLYCOPODIUM CLAVATUMSEVENE USAcf85a896-a004-5b11-e053-2995a90a4df12025-02-11WarningsExact identifier
ndc (package): 76472-3024-1
ndc (product): 76472-3024
ndc11 (package): 76472302401
spl id: 2ddc4f13-eb80-fc5e-e063-6394a90a9792
spl set id: cf85a896-a004-5b11-e053-2995a90a4df1

Reported adverse events (FAERS/openFDA)#

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