NDC 44911-0014 Sp

Brosimum Acutifolium Bark, Himatanthus Sucuuba Bark, Mansoa Alliacea Bark And Leaf, Minquartia Guianenis Bark, Phyllanthus Niruri Whole

NDC Product Code 44911-0014

NDC CODE: 44911-0014

Proprietary Name: Sp 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: Brosimum Acutifolium Bark, Himatanthus Sucuuba Bark, Mansoa Alliacea Bark And Leaf, Minquartia Guianenis Bark, Phyllanthus Niruri Whole 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

NDC 44911-0014-1

Package Description: 120 mL in 1 BOTTLE, DROPPER

NDC Product Information

Sp with NDC 44911-0014 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Sp is brosimum acutifolium bark, himatanthus sucuuba bark, mansoa alliacea bark and leaf, minquartia guianenis bark, phyllanthus niruri whole. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Energique, Inc.

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.

Sp 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.


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.

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: 09-12-2013 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: 12-31-2021 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.

Sp Product Label Images

Sp 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:

Brosimum Acutifolium (Tamamuri) Bark 32X, Himatanthus Sucuuba (Bellaco Caspi) Bark 32X, Mansoa Alliacea (Ajos Sacha) Bark and Leaf 32X,  Minquartia Guianenis (Huacapu) Bark 32X, Phyllanthus Niruri (Phyllanthus/Chanca Piedra) Whole Herb 32X, Piiper Aduncum (Spiked Pepper/Matico) Leaf 32X.


For relief of symptoms of musculoskeletal discomfort.

For relief of symptoms of musculoskeletal discomfort.


​If pregnant or breast-feeding,​ ask a health professional before use. Consult a physician for use in children under 12 years of age.​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.


Adults and children 10 drops under the tongue, twice daily or as directed. If symptoms persist, consult your health care professional.

Inactive Ingredients:

Demineralized Water, 25% Ethanol


​Distributed byChi Research, Inc.207 6th Street SouthWalker, MN 56484218-547-1775

Package Display Label:

​CHI RESEARCHSPHomeopathic Remedy4 fl. oz. (120 ml)

* Please review the disclaimer below.