NDC 62713-921 Progena Adrenal Plus
Atropinum Sulphuricum, Berberis Vulgaris, Bryonia, Carduus Marianus, Chelidonium Majus, Echinacea, Glandula Suprarenalis, Lycopodium Clavatum, Magnesia Phosphorica, Spleen, Zingiber Officinale
NDC Product Code 62713-921
Proprietary Name: Progena Adrenal 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: Atropinum Sulphuricum, Berberis Vulgaris, Bryonia, Carduus Marianus, Chelidonium Majus, Echinacea, Glandula Suprarenalis, Lycopodium Clavatum, Magnesia Phosphorica, Spleen, Zingiber Officinale 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
- 62713-921 - Progena
NDC 62713-921-01
Package Description: 30 mL in 1 BOTTLE, DROPPER
NDC Product Information
Progena Adrenal Plus with NDC 62713-921 is a a human over the counter drug product labeled by Meditrend, Inc. Dba Progena Professional Formulations. The generic name of Progena Adrenal Plus is atropinum sulphuricum, berberis vulgaris, bryonia, carduus marianus, chelidonium majus, echinacea, glandula suprarenalis, lycopodium clavatum, magnesia phosphorica, spleen, zingiber officinale. 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 Adrenal 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.
- ATROPINE SULFATE 6 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
- BRYONIA ALBA ROOT 4 [hp_X]/mL
- SILYBUM MARIANUM SEED 2 [hp_X]/mL
- CHELIDONIUM MAJUS 3 [hp_X]/mL
- ECHINACEA, UNSPECIFIED 2 [hp_X]/mL
- SUS SCROFA ADRENAL GLAND 6 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 8 [hp_X]/mL
- SUS SCROFA SPLEEN 6 [hp_X]/mL
- GINGER 2 [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: 12-31-2018 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: E 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 Adrenal Plus Product Label Images
Progena Adrenal 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:Atropinum Sulphuricum 6X, Berberis Vulgaris 3X, Bryonia 4X, Carduus Marianus 2X, Chelidonium Majus 3X, Echinacea 2X, Glandula Suprarenalis 6X, Lycopodium Clavatum 12X, Magnesia Phosphorica 8X, Spleen 6X, Zingiber Officinale 2X.
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 (12 and Older)take 15 drops under the tongue three times daily.•Children (11 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.
Other Safety Information
Other Information: Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
Inactive Ingredient
Inactive Ingredients:Demineralized water and 25% USP Ethanol.
* Please review the disclaimer below.