NDC 44911-0217 Neurostat
Cimicifuga Racemosa, Agaricus Muscarius, Coccus Cacti, Conium Maculatum, Cuprum Metallicum, Gelsemium Sempervirens, Lycopodium Clavatum, Phosphorus, Rhus Tox, Tarentula Cubensis, Latrodectus Mactans, Pyrogenium Liquid Oral
NDC Product Code 44911-0217
Proprietary Name: Neurostat What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: Cimicifuga Racemosa, Agaricus Muscarius, Coccus Cacti, Conium Maculatum, Cuprum Metallicum, Gelsemium Sempervirens, Lycopodium Clavatum, Phosphorus, Rhus Tox, Tarentula Cubensis, Latrodectus Mactans, Pyrogenium What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 44911 - Energique, Inc.
- 44911-0217 - Neurostat
NDC 44911-0217-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
NDC Product Information
Neurostat with NDC 44911-0217 is a human over the counter drug product labeled by Energique, Inc.. The generic name of Neurostat is cimicifuga racemosa, agaricus muscarius, coccus cacti, conium maculatum, cuprum metallicum, gelsemium sempervirens, lycopodium clavatum, phosphorus, rhus tox, tarentula cubensis, latrodectus mactans, pyrogenium. The product's dosage form is liquid and is administered via oral form.
Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Neurostat Active Ingredient(s)
What is the Active Ingredient(s) List?This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
- AMANITA MUSCARIA FRUITING BODY 12 [hp_X]/mL
- BLACK COHOSH 3 [hp_X]/mL
- CITHARACANTHUS SPINICRUS 12 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
- COPPER 12 [hp_X]/mL
- GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/mL
- LATRODECTUS MACTANS 15 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- PHOSPHORUS 12 [hp_X]/mL
- PROTORTONIA CACTI 12 [hp_X]/mL
- RANCID BEEF 30 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL
Inactive Ingredient(s)
About the Inactive Ingredient(s)The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Administration Route(s)
What are the Administration Route(s)?The translation of the route code submitted by the firm, indicating route of administration.
- Oral - Administration to or by way of the mouth.
Pharmacologic Class(es)
What is a Pharmacological Class?These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.
- Copper - [CS]
- Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
- Decreased Embryonic Implantation - [PE] (Physiologic Effect)
- Decreased Sperm Motility - [PE] (Physiologic Effect)
- Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Energique, Inc.
Labeler Code: 44911
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Start Marketing Date: 07-15-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
* Please review the disclaimer below.
Neurostat Product Label Images
Neurostat Product Labeling Information
The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
Product Labeling Index
- Active Ingredients:
- Indications:
- Warnings:
- Keep Out Of Reach Of Children:
- Directions:
- Inactive Ingredients:
- Questions:
- Package Label Display:
Active Ingredients:
Cimicifuga Racemosa 3X, Agaricus Muscarius 12X, Coccus Cacti 12X, Conium Maculatum 12X, Cuprum Metallicum 12X, Gelsemium Sempervirens 12X, Lycopodium Clavatum 12X, Phosphorus 12X, Rhus Tox 12X, Tarentula Cubensis 12X, Latrodectus Mactans 15X, Pyrogenium 30X.
Indications:
For temporary relief of dizziness when riding or sitting, weak memory, feeling indifferent or confused.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
For temporary relief of dizziness when riding or sitting, weak memory, feeling indifferent or confused.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Warnings:
If pregnant or breast-feeding, ask a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.
Keep Out Of Reach Of Children:
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Directions:
Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.
Inactive Ingredients:
Demineralized water, 20% Ethanol
Questions:
Dist. by Energique, Inc.201 Apple BlvdWoodbine, IA 51579 800-869-8078
Package Label Display:
ENERGIQUESINCE 1987HOMEOPATHIC REMEDYNEUROSTAT1 fl. oz. (30 ml)
* Please review the disclaimer below.