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NDC 50114-7015-02 Engystol 6; 4 [hp_X]/1.1mL; [hp_X]/1.1mL Details
Engystol 6; 4 [hp_X]/1.1mL; [hp_X]/1.1mL
Engystol is a INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by MediNatura. The primary component is CYNANCHUM VINCETOXICUM ROOT; SULFUR.
Product Information
NDC | 50114-7015 |
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Product ID | 50114-7015_cb45601b-173d-4390-bbd2-09476195dca3 |
Associated GPIs | 99870010002200 |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Engystol |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | CYNANCHUM VINCETOXICUM ROOT and SULFUR |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION |
Route | INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Active Ingredient Strength | 6; 4 |
Active Ingredient Units | [hp_X]/1.1mL; [hp_X]/1.1mL |
Substance Name | CYNANCHUM VINCETOXICUM ROOT; SULFUR |
Labeler Name | MediNatura |
Pharmaceutical Class | n/a |
DEA Schedule | n/a |
Marketing Category | UNAPPROVED HOMEOPATHIC |
Application Number | n/a |
Listing Certified Through | n/a |
Package
Package Images

NDC 50114-7015-02 (50114701502)
NDC Package Code | 50114-7015-2 |
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Billing NDC | 50114701502 |
Package | 3 AMPULE in 1 CARTON (50114-7015-2) / 1.1 mL in 1 AMPULE |
Marketing Start Date | 2014-05-31 |
NDC Exclude Flag | N |
Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL a05158b5-ae28-4889-881c-6a7883c96f4c Details
DESCRIPTION
INDICATIONS AND USAGE
DOSAGE AND ADMINISTRATION
General Considerations
• The dosage schedules listed below can be used as a general guide for the administration of Engystol® Injection Solution.
• Engystol® Injection Solution may be administered s.c., i.d., i.m., or i.v.
• The interval between injections is left to the discretion of the HCP, but should not exceed 1 ampule in 24 hours.
• Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Discard any unused ampule contents.
• Draw up required dose into syringe.
• Discard any unused ampule contents. Do not reuse ampule.
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Only licensed practitioners with sufficient expertise in injecting drugs, including the respective route of administration, should administer the product.
Standard Dosage:
Adults and children 12 years and older: 1 ml 1 to 3 times per 7 days.
Children 6 to 11 years: 0.7 ml 1 to 3 times per 7 days.
Children 2 to 5 years: 0.5 ml 1 to 3 times per 7 days.
Acute Dosage:
Adults and children 12 years and older: 1 ml daily, and then continue with standard dosage.
Children 6 to 11 years: 0.7 ml daily, and then continue with standard dosage.
Children 2 to 5 years: 0.5 ml daily, and then continue with standard dosage.
CONTRAINDICATIONS
ADVERSE REACTIONS
Post-marketing Experience
• The following adverse events have been identified during post-marketing use of Engystol® Injection Solution. Because these events are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
• Allergic (hypersensitivity) skin reactions may occur in isolated cases.
To report SUSPECTED ADVERSE REACTIONS, contact MediNatura. at 1.844.633.4628 or [email protected] or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch
OVERDOSAGE
CLINICAL PHARMACOLOGY
DOSAGE
INGREDIENTS AND APPEARANCE
ENGYSTOL
cynanchum vincetoxicum root and sulfur injection |
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Labeler - MediNatura (102783016) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
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Hameln Pharma GmbH | 315869123 | manufacture(50114-7015) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
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Biologische Heilmittel Heel | 315635359 | manufacture(50114-7015) |