Colocynthis Homaccord

Manufacturer
JENAHEXAL PHARMA GMBH
Effective date
2009-09-09
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:02:46

Label at a glance#

ProductColocynthis Homaccord
Active ingredientGNAPHALIUM, CITRULLUS COLOCYNTHIS FRUIT WITHOUT SEED
Label structure15 sections

Storage and handling

9.     Storage Conditions      9.1    Avoid freezing and excessive heat. Store at room temperature. Protect from light.

Label contents#

Full prescribing information#

DESCRIPTION SECTION

Description:
     •        Injection Solution Ingredient Information: Each 1.1ml ampule contains: Gnaphalium polycephalum 3X,10X,30X,200X 2.2mcl each; Colocynthis 4X,10X,30X,200X 8.8mcl each. Inactive ingredient: Sterile isotonic sodium chloride solution.

INDICATIONS & USAGE SECTION

Indications and Usage:
     •        Colocynthis-Homaccord® Injection Solution is indicated for neuralgia of various origins and locations, especially sciatic neuralgia, intercostal neuralgia and intervertebral disc disorders.

DOSAGE & ADMINISTRATION SECTION

Dosage and Administration:
     •     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 ½ the adult dosage. (2.1)

DOSAGE FORMS & STRENGTHS SECTION

Dosage Form and Strength:
     •     Injections: 1.1ml ampule

WARNINGS AND PRECAUTIONS SECTION

Warnings and Precautions
    If pain persists or worsens, if new symptoms occur, or if redness or swelling is present, the patient should be carefully re-evaluated because  these could be signs of a serious condition.
     •     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.
     •     To report SUSPECTED ADVERSE REACTIONS, contact Heel Inc. at 1.800.920.9203 or info@heelusa.com or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

INDICATIONS & USAGE SECTION

1.     Indications and Usage
     1.1    Colocynthis-Homaccord® Injection Solution is classifed as a homeopathic combination drug.
     1.2    Botanical ingredients: Colocynthis (bitter cucumber) Gnaphalium polycephalum (common everlasting)
     1.3    Colocynthis-Homaccord® Injection Solution is indicated for neuralgia of various origins and locations, especially sciatic neuralgia, intercostal neuralgia and intervertebral disc disorders.

DOSAGE & ADMINISTRATION SECTION

2.     Dosage and Administration
     2.1     The dosage schedules listed below can be used as a general guide for the administration of Colocynthis-Homaccord® Injection Solution. Colocynthis-Homaccord® Injection Solution shows individual differences in clinical response. Therefore, the dosage for each patient should be individualized according to the patient’s response to 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 ½ the adult dosage.    
                            
Discard unused solution.

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

WARNINGS AND PRECAUTIONS SECTION

3.        Warnings and Precautions    
     3.1    Colocynthis-Homaccord® Injection Solution exhibits no known adverse renal, hepatic, cardiovascular, gastrointestinal or central nervous system effects.
     3.2    No harmful or potentially harmful side effects such as central nervous system depression are known. Colocynthis-Homaccord® Injection Solution is generally well-tolerated, however, if symptoms persist or worsen discontinue use.
     3.3    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.
     3.4    Drug Interactions: None known
     3.5    Drug / Laboratory Test Interaction: None known
     3.6    Carcinogenesis, mutagenesis, impairment of fertility: Not applicable

 

USE IN SPECIFIC POPULATIONS SECTION

4.     Use in Specifc Populations
     4.1    Pediatric Use: Colocynthis-Homaccord® Injection Solution can be safely administered to children as young as 2 years. (see Dosage and Administration)
     4.2    Nursing Mothers: It is not known whether any of the ingredients in Colocynthis-Homaccord® Injection Solution are excreted in human milk. However, because many drugs are excreted in human milk, Colocynthis-Homaccord® Injection Solution should be administered with caution to nursing mothers.
     4.3    Geriatric use: Colocynthis-Homaccord® Injection Solution is safe to use in adults 12 years and older. (see Dosage and Administration)

CLINICAL PHARMACOLOGY SECTION

5.     Clinical  Pharmacology
     5.1     The exact mechanism of action of Colocynthis-Homaccord® Injection Solution is not fully understood.

DRUG ABUSE AND DEPENDENCE SECTION

6.     Drug Abuse and Dependence
     6.1    Not applicable for homeopathic drugs

OVERDOSAGE SECTION

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

HOW SUPPLIED SECTION

8.     How Supplied
     8.1    Colocynthis-Homaccord® Injection Solution 1.1ml ampules: Packs of 10 ampules: NDC 50114-7065-1

STORAGE AND HANDLING SECTION

9.     Storage Conditions
     9.1    Avoid freezing and excessive heat. Store at room temperature. Protect from light.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


ColocynthisHoma_Inj_Box.jpg

ColocynthisHoma_Inj_Box.jpg
ColocynthisHoma_Inj_Box.jpg


ColocynthisHoma_Inj insert_Rx2.jpg

ColocynthisHoma_Inj insert_Rx2.jpg
ColocynthisHoma_Inj insert_Rx2.jpg

ColocynthisHoma_Inj insert_Rx.jpg

ColocynthisHoma_Inj insert_Rx.jpgColocynthisHoma_Inj insert_Rx.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68275-320-102019-10-21C16284748780-1956f9ecf-bbfe-621f-e053-dbdaa90a74adColocynthis Homaccord

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68275-320-10Colocynthis Homaccord1.1 mL in 1 AMPULEINJECTION1.11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68275-320COLOCYNTHIS HOMACCORD (GNAPHALIUM AND CITRULLUS COLOCYNTHIS FRUIT WITHOUT SEED) INJECTION [JENAHEXAL PHARMA GMBH ]1Legacy NDC, 1 package rows20110113_05f405bb-6933-44a1-ab48-05faf19fbb4d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CITRULLUS COLOCYNTHIS FRUIT WITHOUT SEEDACTIVE INGREDIENT23H32AOH171
GNAPHALIUMACTIVE INGREDIENTBGI20Z6M571
CITRULLUS COLOCYNTHIS FRUIT WITHOUT SEEDACTIVE MOIETY23H32AOH171
GNAPHALIUMACTIVE MOIETYBGI20Z6M571

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
68275-32068275-320-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
2e956093-0266-4a5a-8926-610a8ff7cdfd05f405bb-6933-44a1-ab48-05faf19fbb4d2009-09-09WarningsExact identifier
spl id: 2e956093-0266-4a5a-8926-610a8ff7cdfd
spl set id: 05f405bb-6933-44a1-ab48-05faf19fbb4d

Reported adverse events (FAERS/openFDA)#

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