Lymphomyosot 1.1ml Injection

Manufacturer
Hameln Pharma GmbH
Effective date
2010-04-01
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:53:04

Label at a glance#

ProductLymphomyosot
Active ingredientGERANIUM ROBERTIANUM, RORIPPA NASTURTIUM-AQUATICUM, FERROUS IODIDE, JUGLANS REGIA FLOWERING TOP, MYOSOTIS ARVENSIS, SCROPHULARIA NODOSA, TEUCRIUM SCORODONIA FLOWERING TOP, VERONICA OFFICINALIS FLOWERING TOP, EQUISETUM HYEMALE, FUMARIA OFFICINALIS FLOWERING TOP, SODIUM SULFATE, PINUS SYLVESTRIS TOP, GENTIANA LUTEA ROOT, ARANEUS DIADEMATUS, SARSAPARILLA, TRIBASIC CALCIUM PHOSPHATE, LEVOTHYROXINE
Label structure9 sections

Dosage and administration

The dosage schedules listed can be used as a general guide for the administration of Lymphomyosot ® Injection Solution. Lymphomyosot ® Injection Solution shows individual differences in clinical response. Therefore, the dosage for each patient should be individualized according to the patient's response therapy. Adults and children 7 years and older: in acute disorders, 1 ampule per day, otherwise 1 ampule, 1 to 3...

Storage and handling

Avoid freezing and excessive heat. Store at room temperature. Protect from light.

Label contents#

Full prescribing information#

DESCRIPTION

DESCRIPTION SECTION

Injection Solution Ingredient Information: Each 1.1ml ampule contains: Geranium robertianum 4X 1.1 mcl, Nasturtium aquaticum 4X 1.1 mcl, Ferrum iodatum 12X 1.1 mcl, Juglans regia 3X 0.55 mcl, Myosotis arvensis 3X 0.55 mcl, Scrophularia nodosa 3X 0.55 mcl, Teucrium scorodonia 3X 0.55 mcl, Veronica officinalis 3X 0.55 mcl, Equistetum hyemale 4X 0.55 mcl, Fumaria officinalis 4X 0.55 mcl, Natrum sulphuricum 4X 0.55 mcl, Pinus sylvestris 4X 0.55 mcl, Gentiana lutea 5X 0.55 mcl, Aranea diadema 6X 0.55 mcl, Sarsaparilla 6X 0.55 mcl, Calcarea phosphorica 12X 0.55 mcl, Levothyroxine 12X 0.55 mcl. Inactive Ingredients: Sterile Isotonic sodium chloride solution.

INDICATION AND USAGE

INDICATIONS & USAGE SECTION

Lymphomyosot® Injection Solution is classified as a homeopathic combination drug.

Botanical Ingredients:
Equisetum hyemale (Horsetail), Fumaria officinalis (Common fumitory), Gentiana lutea (Yellow gentian), Geranium robertianum (Herb Robert), Juglans regia (Walnut), Myosotis arvensis (Forget-me-not), Nasturtium aquaticum (Watercress), Pinus sylvestris (Scotch Pine), Sarsaparilla (Wild liquorice), Scrophularia nodosa (Figwort), Teucrium scorodonia (Wood-germander), Veronica officinalis (Common speedwell).

Mineral Ingredients:
Calcarea phosphorica (Tribasic calcium phosphate), Ferrum iodatum (Ferrous iodide), Natrum sulphuricum (Disodium sulfate).

Animal-derived ingredients:
Aranea diadema (Papal-cross spider), Levothyroxine (L-thyroxine).

Lymphomyosot® Injection Solution is indicated for the temporary relief of swelling due to poor circulation, minor injury and environmental toxins.
 

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

The dosage schedules listed can be used as a general guide for the administration of Lymphomyosot® Injection Solution. Lymphomyosot® Injection Solution shows individual differences in clinical response. Therefore, the dosage for each patient should be individualized according to the patient's response therapy.

Adults and children 7 years and older: in acute disorders, 1 ampule per day, otherwise 1 ampule, 1 to 3 times per week IM/SC/IV/ID. Children ages 2 to 6: receive 1/2 the adult dosage. Discard unused solution.

Lymphomyosot® Injection Solution may be administered intravenously, intramuscularly, subcutaneously, or intradermally. The required dose of Lymphomyosot® Injection Solution is first withdrawn from the ampule into the syringe, and the syringe is then shaken briefly. Lymphomyosot® Injection Solution should be administered using a narrow gauge needle (e.g. 22 to 30 gauge). Note: Parental drug products like Lymphomyosot® Injection Solution should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit. Lymphomyosot® Injection Solution is a clear, colorless solution. Discolored solutions should be discarded.

WARNINGS AND PRECAUTIONS

WARNINGS AND PRECAUTIONS SECTION

If new syptoms occur, or if redness, pain or swelling at the puncture site persists, the patient should be carefully re-evaluated because these could be signs of a more serious condition.

Lymphomyosot® Injection Solution exhibits no known adverse renal, hepatic, cardiovascular, gastrointestinal or central nervous system side effects.


No harmful or potentially harmful side effects such as central nervous system depression are known. Lymphomyosot® Injection Solution is generally well-tolerated, however, if symptoms persist or worsen discontinue use.


Teratogenic effects: In general, homeopathic drugs are not known to cause direct or indirect harm to the fetus Pregnancy Category C. Animal reproduction studies have not been conducted with this drug. It is also not known whether this drug can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. This drug should be given to a pregnant woman only if clearly needed.

Drug Interactions: None known

Drug/Laboratory Test Interaction: None known

Carcinogenesis, mutagenesis, impairment of fertility: Not applicable

OVERDOSAGE

OVERDOSAGE SECTION

Due to the low concentration of active ingredients in homeopathic preparations such as Lymphomyosot® Injection Solution. adverse reactions following over dosage are extremely unlikely. However, care must be taken not to exceed the recommended dosage.



CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

The exact mechanism of action of Lymphomyosot® Injection Solution is not fully understood.

DOSAGE

DOSAGE FORMS & STRENGTHS SECTION

Injections: 1.1 ml ampule

STORAGE CONDITIONS

STORAGE AND HANDLING SECTION

Avoid freezing and excessive heat. Store at room temperature. Protect from light.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


Lymphomyosot_injectable box.jpgLymphomyosot_injectable box.jpg

Lymphomyosot_injectable box.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52919-123-102025-11-17C16284748780-1956f9ecf-ce2b-621f-e053-dbdaa90a74adLymphomyosot 1.1ml Injection
52919-123-102019-10-21C16284748780-1956f9ecf-ce2b-621f-e053-dbdaa90a74adLymphomyosot 1.1ml Injection

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52919-123LYMPHOMYOSOT (GERANIUM ROBERTIANUM AND RORIPPA NASTURTIUM-AQUATICUM AND TRIBASIC CALCIUM PHOSPHATE AND LEVOTHYROXINE AND ) INJECTION [HAMELN PHARMA GMBH]1Legacy NDC20100608_8b9820bb-d592-46bf-b1db-f91947bf49aa.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARANEUS DIADEMATUSACTIVE INGREDIENT6T6CO7R3Z51
EQUISETUM HYEMALEACTIVE INGREDIENT59677RXH251
FERROUS IODIDEACTIVE INGREDIENTF5452U54PN1
FUMARIA OFFICINALIS FLOWERING TOPACTIVE INGREDIENTVH659J61ZL1
GENTIANA LUTEA ROOTACTIVE INGREDIENTS72O3284MS1
GERANIUM ROBERTIANUMACTIVE INGREDIENTR5I1HK0UBL1
JUGLANS REGIA FLOWERING TOPACTIVE INGREDIENT3BA2N709NG1
LEVOTHYROXINEACTIVE INGREDIENTQ51BO43MG41
MYOSOTIS ARVENSISACTIVE INGREDIENTC73BK97H5J1
PINUS SYLVESTRIS TOPACTIVE INGREDIENTQ1RGP4UB731
RORIPPA NASTURTIUM-AQUATICUMACTIVE INGREDIENTYH89GMV6761
SARSAPARILLAACTIVE INGREDIENT2H1576D5WG1
SCROPHULARIA NODOSAACTIVE INGREDIENT7H443NUB2T1
SODIUM SULFATEACTIVE INGREDIENT0YPR65R21J1
TEUCRIUM SCORODONIA FLOWERING TOPACTIVE INGREDIENTLOK3I16O7G1
TRIBASIC CALCIUM PHOSPHATEACTIVE INGREDIENT91D9GV0Z281
VERONICA OFFICINALIS FLOWERING TOPACTIVE INGREDIENT9IH82J936J1
ARANEUS DIADEMATUSACTIVE MOIETY6T6CO7R3Z51
CALCIUM CATIONACTIVE MOIETY2M83C4R6ZB1
EQUISETUM HYEMALEACTIVE MOIETY59677RXH251
FERROUS IODIDEACTIVE MOIETYF5452U54PN1
FUMARIA OFFICINALIS FLOWERING TOPACTIVE MOIETYVH659J61ZL1
GENTIANA LUTEA ROOTACTIVE MOIETYS72O3284MS1
GERANIUM ROBERTIANUMACTIVE MOIETYR5I1HK0UBL1
JUGLANS REGIA FLOWERING TOPACTIVE MOIETY3BA2N709NG1
LEVOTHYROXINEACTIVE MOIETYQ51BO43MG41
MYOSOTIS ARVENSISACTIVE MOIETYC73BK97H5J1
PINUS SYLVESTRIS TOPACTIVE MOIETYQ1RGP4UB731
RORIPPA NASTURTIUM-AQUATICUMACTIVE MOIETYYH89GMV6761
SARSAPARILLAACTIVE MOIETY2H1576D5WG1
SCROPHULARIA NODOSAACTIVE MOIETY7H443NUB2T1
SODIUM CATIONACTIVE MOIETYLYR4M0NH371
TEUCRIUM SCORODONIA FLOWERING TOPACTIVE MOIETYLOK3I16O7G1
VERONICA OFFICINALIS FLOWERING TOPACTIVE MOIETY9IH82J936J1

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52919-12352919-123-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
41e7ce28-9538-3cfc-e063-6294a90a277a8b9820bb-d592-46bf-b1db-f91947bf49aa2025-10-24WarningsExact identifier
spl set id: 8b9820bb-d592-46bf-b1db-f91947bf49aa

Reported adverse events (FAERS/openFDA)#

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