NDC 62713-966 Progena Tick Bite Support

Avena Sativa, Carduus Marianus, Scrophularia Nodosa, Solidago Virgaurea, Arsenicum Album, Cina, Conium Maculatum, Gelsemium Sempervirens, Lycopodium Clavatum, Mercuris Vivus, Phosphoricum Acidum, Phosphorus, Selenium Metallicum

NDC Product Code 62713-966

NDC CODE: 62713-966

Proprietary Name: Progena Tick Bite Support 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: Avena Sativa, Carduus Marianus, Scrophularia Nodosa, Solidago Virgaurea, Arsenicum Album, Cina, Conium Maculatum, Gelsemium Sempervirens, Lycopodium Clavatum, Mercuris Vivus, Phosphoricum Acidum, Phosphorus, Selenium Metallicum 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

  • 62713 - Meditrend, Inc. Dba Progena Professional Formulations

NDC 62713-966-01

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Progena Tick Bite Support with NDC 62713-966 is a a human over the counter drug product labeled by Meditrend, Inc. Dba Progena Professional Formulations. The generic name of Progena Tick Bite Support is avena sativa, carduus marianus, scrophularia nodosa, solidago virgaurea, arsenicum album, cina, conium maculatum, gelsemium sempervirens, lycopodium clavatum, mercuris vivus, phosphoricum acidum, phosphorus, selenium metallicum. The product's dosage form is liquid and is administered via oral form.

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.

Progena Tick Bite Support 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: Meditrend, Inc. Dba Progena Professional Formulations
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: 10-15-2021 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: 12-31-2022 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.

Progena Tick Bite Support Product Label Images

Progena Tick Bite Support 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

Active Ingredients: Avena sativa 3X, Carduus marianus 3X, Solidago virgaurea 3X, Scrophularia nodosa 8X, Arsenicum album 30C, Cina 30C, Conium maculatum 30C, Gelsemium sempervirens 30C, Lycopodium clavatum 30C, Mercuris vivus 30C, Phosphoricum acidum 30C, Phosphorus 30C, Selenium metallicum 30C.

Otc - Purpose

Purpose:Promotes Immune Function to support symptoms from tick bites.

Indications & Usage

Use: This product is a homeopathic dilution formulated to promote immunity when experiencing symptoms from tick bites.*

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: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


Adults (12 and Older) 15 drops under the tongue three times daily.•

Children (Under 12) 6 drops under the tongue three times daily or as directed by your health care professional. •

Consult a Physician for 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.