NDC 71781-0006 Homeoplex L

Beta Vulgaris, Carduus Marianus, Taraxacum Officinale, Cholesterinum, Fel Tauri, Chelidonium Majus, Lycopodium Clavatum, Natrum Sulphuricum, Nux Vomica, Phosphorus

NDC Product Code 71781-0006

NDC CODE: 71781-0006

Proprietary Name: Homeoplex L 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: Beta Vulgaris, Carduus Marianus, Taraxacum Officinale, Cholesterinum, Fel Tauri, Chelidonium Majus, Lycopodium Clavatum, Natrum Sulphuricum, Nux Vomica, Phosphorus 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

  • 71781 - Supplement Clinic, Llc.

NDC 71781-0006-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Homeoplex L with NDC 71781-0006 is a a human over the counter drug product labeled by Supplement Clinic, Llc.. The generic name of Homeoplex L is beta vulgaris, carduus marianus, taraxacum officinale, cholesterinum, fel tauri, chelidonium majus, lycopodium clavatum, natrum sulphuricum, nux vomica, phosphorus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Supplement Clinic, Llc.

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.

Homeoplex L 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.

  • BETA VULGARIS 3 [hp_X]/mL
  • MILK THISTLE 3 [hp_X]/mL
  • CHOLESTEROL 6 [hp_X]/mL
  • BOS TAURUS BILE 6 [hp_X]/mL
  • SODIUM SULFATE 12 [hp_X]/mL
  • PHOSPHORUS 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)

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: Supplement Clinic, Llc.
Labeler Code: 71781
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: 11-01-2017 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Homeoplex L Product Label Images

Homeoplex L 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:

Beta Vulgaris 3X, Carduus Marianus 3X, Taraxacum Officinale 3X, Cholesterinum 6X, Fel Tauri 6X, Chelidonium Majus 12X, Lycopodium Clavatum 12X, Natrum Sulphuricum 12X, Nux Vomica 12X, Phosphorus 12X.


For general liver support.

For general liver support.


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 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.


1 drop orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional.

Inactive Ingredients:

Demineralized Water, Glycerin


Distributed By:Supplement Clinic, LLC. • Kelso, WA 986261(800)691-9009 • www.supplementclinic.com

Package Label Display:

LAM MDFoundational NutritionHomeoPlex LHOMEOPATHIC2 FL OZ (60 ml)

* Please review the disclaimer below.