NDC 57520-0254 Adrenapar
Aralia Quinquefolia, Avena Sativa Glandula Suprarenalis, Arsenicum Iodatum, Ignatia Amara, Lycopodium Clavatum, Nux Vomica, Liquid Oral

Product Information

Product Code57520-0254
Proprietary Name 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.
Adrenapar
Non-Proprietary Name 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.
Aralia Quinquefolia, Avena Sativa Glandula Suprarenalis, Arsenicum Iodatum, Ignatia Amara, Lycopodium Clavatum, Nux Vomica,
Product Type 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.
Human Otc Drug
Dosage FormLiquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Apotheca Company
Labeler Code57520
Marketing Category 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.
UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
10-05-2010
End Marketing Date What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
09-12-2022
Exclude Flag 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".
N
NDC Code Structure

Usage Information


Product Packages

NDC 57520-0254-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

Product Details

Adrenapar is a human over the counter drug product labeled by Apotheca Company. The generic name of Adrenapar is aralia quinquefolia, avena sativa glandula suprarenalis, arsenicum iodatum, ignatia amara, lycopodium clavatum, nux vomica, . The product's dosage form is liquid and is administered via oral form.


What are Adrenapar Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.


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)


Pharmacologic Class(es)

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.


* Please review the disclaimer below.

Adrenapar Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Otc - Active Ingredient



ACTIVE INGREDIENTS:  Aralia quinquefolia 3X, Avena sativa 3X, Glandula suprarenalis 6X, Arsenicum iodatum 12X, Ignatia amara 12X, Lycopodium clavatum 12X, Nux vomica 12X, Phosphoricum acidum 12X, Phosphorus 12X, Zincum metallicum 12X.


Otc - Purpose



INDICATIONS:  For temporary relief of nervous exhaustion, fatigue and forgetfulness.



Warnings



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.



Dosage & Administration



SUGGESTED USE:  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 Ingredient



INACTIVE INGREDIENTS:  Demineralized water, 20% Ethanol



Otc - 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.



Indications & Usage



INDICATIONS:  For temporary relief of nervous exhaustion, fatigue and forgetfulness.



Otc - Questions



Dist.by  Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579

800-869-8078



Package Label.Principal Display Panel



ENERGIQUE

ADRENAPAR

Homeopathic Remedy

2 fl. oz (60 ml)


* Please review the disclaimer below.