NDC 43857-0427 Pacreaplex

Chelidonium Majus, Glycyrrhiza Glabra, Nux Moschata, Rheum (officinale), Syzygium Jambolanum, Taraxacum Officinale, Zingiber Officinale, Hydrastis Canadensis, Glandula Suprarenalis Suis, Hepar Suis, Hypophysis Suis, Pancreas Suis, Thyroidinum (suis), Phaseolus, Phosphoricum Acidum, Phosphorus

NDC Product Code 43857-0427

NDC Code: 43857-0427

Proprietary Name: Pacreaplex 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: Chelidonium Majus, Glycyrrhiza Glabra, Nux Moschata, Rheum (officinale), Syzygium Jambolanum, Taraxacum Officinale, Zingiber Officinale, Hydrastis Canadensis, Glandula Suprarenalis Suis, Hepar Suis, Hypophysis Suis, Pancreas Suis, Thyroidinum (suis), Phaseolus, Phosphoricum Acidum, 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

  • 43857 - Bioactive Nutritional, Inc.
    • 43857-0427 - Pacreaplex

NDC 43857-0427-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Pacreaplex with NDC 43857-0427 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Pacreaplex is chelidonium majus, glycyrrhiza glabra, nux moschata, rheum (officinale), syzygium jambolanum, taraxacum officinale, zingiber officinale, hydrastis canadensis, glandula suprarenalis suis, hepar suis, hypophysis suis, pancreas suis, thyroidinum (suis), phaseolus, phosphoricum acidum, phosphorus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Bioactive Nutritional, 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.

Pacreaplex 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.

  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • GLYCYRRHIZA GLABRA 3 [hp_X]/mL
  • NUTMEG 3 [hp_X]/mL
  • RHEUM OFFICINALE ROOT 3 [hp_X]/mL
  • SYZYGIUM CUMINI SEED 3 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL
  • GINGER 3 [hp_X]/mL
  • GOLDENSEAL 5 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 6 [hp_X]/mL
  • PORK LIVER 6 [hp_X]/mL
  • SUS SCROFA PITUITARY GLAND 6 [hp_X]/mL
  • SUS SCROFA PANCREAS 6 [hp_X]/mL
  • SUS SCROFA THYROID 8 [hp_X]/mL
  • KIDNEY BEAN 12 [hp_X]/mL
  • PHOSPHORIC ACID 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)
  • 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: Bioactive Nutritional, Inc.
Labeler Code: 43857
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: 01-24-2017 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: 12-31-2019 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.

Pacreaplex Product Label Images

Pacreaplex 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:

Chelidonium Majus 3X, Glycyrrhiza Glabra 3X, Nux Moschata 3X, Rheum (Officinale) 3X, Syzygium Jambolanum 3X, Taraxacum Officinale 3X, Zingiber Officinale 3X, Hydrastis Canadensis 5X, Glandula Suprarenalis Suis 6X, Hepar Suis 6X, Hypophysis Suis 6X, Pancreas Suis 6X, Thyroidinum (Suis) 8X, Phaseolus 12X, Phosphoricum Acidum 12X, Phosphorus 12X.

Indications:

For temporary relief of nervous anxiety, afternoon headache, feeling faint relieved by eating, craving of sweets, nervousness if meals missed.

For temporary relief of nervous anxiety, afternoon headache, feeling faint relieved by eating, craving of sweets, nervousness if meals missed.

Warnings:

If pregnant or breast-feeding, ask a health care 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.

Directions:

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Distributed by:BioActive Nutritional, Inc.1803 N. Wickham Rd.Melbourne, FL 32935bioactivenutritional.com

Package Label Display:

BIOActive NutritionalPANCREAPLEXHOMEOPATHIC1 FL OZ (30 ml)

* Please review the disclaimer below.

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