NDC 62713-914 Progena Pancreas Plus
Acidum Phosphoricum, Berberis Vulgaris, Bilberry, Cheidonium Majus, Creosotum, Kidney, Natrum Sulpuricum, Pancreas, Syzygium Jambolanum
NDC Product Code 62713-914
Proprietary Name: Progena Pancreas Plus 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: Acidum Phosphoricum, Berberis Vulgaris, Bilberry, Cheidonium Majus, Creosotum, Kidney, Natrum Sulpuricum, Pancreas, Syzygium Jambolanum 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.
Code Structure
- 62713 - Meditrend, Inc. Dba Progena Professional Formulations
- 62713-914 - Progena
NDC 62713-914-01
Package Description: 30 mL in 1 BOTTLE, DROPPER
NDC Product Information
Progena Pancreas Plus with NDC 62713-914 is a a human over the counter drug product labeled by Meditrend, Inc. Dba Progena Professional Formulations. The generic name of Progena Pancreas Plus is acidum phosphoricum, berberis vulgaris, bilberry, cheidonium majus, creosotum, kidney, natrum sulpuricum, pancreas, syzygium jambolanum. The product's dosage form is liquid and is administered via oral form.
Labeler Name: Meditrend, Inc. Dba Progena Professional FormulationsDosage 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.
Progena Pancreas Plus 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.
- PHOSPHORIC ACID 4 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 2 [hp_X]/mL
- BILBERRY 2 [hp_X]/mL
- CHELIDONIUM MAJUS 4 [hp_X]/mL
- WOOD CREOSOTE 6 [hp_X]/mL
- PORK KIDNEY 6 [hp_X]/mL
- SODIUM SULFATE 6 [hp_X]/mL
- SUS SCROFA PANCREAS 6 [hp_X]/mL
- SYZYGIUM CUMINI SEED 10 [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 Code: 62713
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: 01-01-1985 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.
Progena Pancreas Plus Product Label Images
Progena Pancreas Plus 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
- Otc - Active Ingredient
- Otc - Purpose
- Indications & Usage
- Otc - Keep Out Of Reach Of Children
- Warnings
- Dosage & Administration
- Other Safety Information
- Inactive Ingredient
Otc - Active Ingredient
Active Ingredients:Acidum Phosphoricum 4X, Berberis Vulgaris 2X, Bilberry 2X, Cheidonium Majus 4X, Creosotum 6X, Kidney 6X, Natrum sulpuricum 6X, Pancreas 6X, Syzygium Jambolanum 10X.
Otc - Purpose
Purpose:Support for the Body's Endocrine and Organ System.
Indications & Usage
Use:This product is a Homeopathic Dilution, formulated to support the Body's Endocrine and Organ System.
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.
Warnings
- Warnings:Use Only as directed.Stop use and ask a doctor ifsymptoms worsen or do not improve after 5 days.
- If pregnant or breast-feeding, consult a health professional before use.
Dosage & Administration
Directions:•
Adults (13 and Older)take 15 drops under the tongue three times daily.•
Children (12 and Younger)take 10 drops under the tongue three times daily or as directed by your health care professional.•
Consult a Physicianfor use in children under 12 years of age.•
Not Recommendedfor children under 2 years of age.
Other Safety Information
Other Information: Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
Inactive Ingredient
Inactive Ingredients:USP Purified Water and 25% USP Ethanol.
* Please review the disclaimer below.