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  4. NDC Product Code: 57520-0251 11 Thyroid Adrenal

NDC 57520-0251 11 Thyroid Adrenal

Iodium,Phytolacca Decandra,Adrenalinum,Adrenocorticotrophin,Belladonna,Thyroidinum,Natrum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57520-0251?
  4. 11 Thyroid Adrenal Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 57520-0251 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
57520-0251
Proprietary Name:
11 Thyroid Adrenal
Non-Proprietary Name: [1]
Iodium, Phytolacca Decandra, Adrenalinum, Adrenocorticotrophin, Belladonna, Thyroidinum, Natrum Muriaticum,
Substance Name: [2]
Atropa Belladonna; Corticotropin; Epinephrine; Iodine; Nutmeg; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Phytolacca Americana Root; Silver Nitrate; Sodium Chloride; Thyroid, Unspecified
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Lipstick - A waxy solid, usually colored cosmetic, in stick form for the lips.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
Apotheca Company
Labeler Code:
57520
Product Label ID:
24292987-5ee6-4305-b8e3-b4c662c9b04f
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
08-03-2010
End Marketing Date: [10]
07-19-2025
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 57520-0251?

The NDC code 57520-0251 is assigned by the FDA to the product 11 Thyroid Adrenal which is a human over the counter drug product labeled by Apotheca Company. The generic name of 11 Thyroid Adrenal is iodium, phytolacca decandra, adrenalinum, adrenocorticotrophin, belladonna, thyroidinum, natrum muriaticum, . The product's dosage form is lipstick and is administered via oral form. The product is distributed in a single package with assigned NDC code 57520-0251-1 30 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for 11 Thyroid Adrenal?

This product is used as INDICATIONS:  For the temporary relief of confusion and paranoia.

What are 11 Thyroid Adrenal Active Ingredients?

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.
  • ATROPA BELLADONNA 30 [hp_C]/mL - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
  • CORTICOTROPIN 6 [hp_X]/mL
  • EPINEPHRINE 6 [hp_X]/mL - The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
  • IODINE 3 [hp_X]/mL - A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
  • NUTMEG 1 [hp_M]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 1 [hp_M]/mL
  • PHOSPHORUS 1 [hp_M]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/mL
  • SILVER NITRATE 1 [hp_M]/mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
  • SODIUM CHLORIDE 200 [hp_C]/mL - A ubiquitous sodium salt that is commonly used to season food.
  • THYROID, UNSPECIFIED 30 [hp_C]/mL

Which are 11 Thyroid Adrenal UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are 11 Thyroid Adrenal Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes for 11 Thyroid Adrenal?

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.

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Product Footnotes

[1] 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.

[2] What is the Substance Name? - 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.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] 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.

[9] 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] 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.

[12] 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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".