LYCOPODIUM HP

Manufacturer
Natural Creations, Inc | OHM Pharma, Inc.
Effective date
2025-12-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:35:58

Label at a glance#

ProductLYCOPODIUM HP
Active ingredientAMANITA MUSCARIA FRUITING BODY, ONION, ARNICA MONTANA, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, PHOSPHORUS, LEAD
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*) - equal amounts of: Agaricus Muscarius 30X, Allium Cepa 30X, Arnica Montana 30X, Hypericum Perforatum 30X, Lycopodium Clavatum 30X, Mercurius Solubilis 30X, Phosphorus 30X, Plumbum Metallicum 30X.

OTC - PURPOSE SECTION

USES: Temporarily relieves twitching, itching, pain, & tingling in muscles, legs, and feet.**

INDICATIONS & USAGE SECTION

USES: Temporarily relieves twitching, itching, pain, & tingling in muscles, legs, and feet.**

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

WARNINGS SECTION

WARNINGS:

  • Consult a physician for use in children under 12 years of age.
  • IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
  • KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
  • Do not use if TAMPER EVIDENT seal is broken or missing.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Purified Water, Ethyl Alcohol USP.

OTC - QUESTIONS SECTION

QUESTIONS & COMMENTS?

Natural Creations, Inc. / Woodbine, IA 5159 / 712-647-1600

REFERENCES SECTION

*The letters "HPUS" indicate the component in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.

**Claims based on tradtional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0635-1

LYCOPODIUM HP

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130877730004727GTIN-13: 0877730004727
EAN-13: 0877730004727
GTIN-12: 877730004727
UPC-A: 877730004727
GTIN storage (14 digits): 00877730004727
LYCOPODIUM HP.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0635-12023-01-10C16284748780-1d6a99b39-6c57-a426-e053-dadaa90af4c2LYCOPODIUM HP
43406-0635-12022-01-28C16284748780-1d6a99b39-6c57-a426-e053-dadaa90af4c2LYCOPODIUM HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0635-1LYCOPODIUM HP30 mL in 1 BOTTLE, DROPPERLIQUID303

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-063543406-0635-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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 HPAMANITA MUSCARIA FRUITING BODY, ONION, ARNICA MONTANA, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, PHOSPHORUS, LEADNatural Creations, Inc3f477ed2-1e5e-480e-9cde-121d32c4d0752025-12-16WarningsExact identifier
ndc (package): 43406-0635-1
ndc (product): 43406-0635
ndc11 (package): 43406063501
spl id: 6156a3f4-b424-45f6-8c4f-c852016fe1e7
spl set id: 3f477ed2-1e5e-480e-9cde-121d32c4d075

Reported adverse events (FAERS/openFDA)#

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