NDC 68703-353 Vertifree

Bryonia, Cocculus, Gesemium, Lobelia

NDC Product Code 68703-353

NDC CODE: 68703-353

Proprietary Name: Vertifree 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: Bryonia, Cocculus, Gesemium, Lobelia 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.

Product Characteristics

WHITE (C48325)
Shape: ROUND (C48348)
6 MM
Score: 1

NDC Code Structure

  • 68703 - Silver Star Brands

NDC 68703-353-80

Package Description: 180 TABLET in 1 BOTTLE, GLASS

NDC Product Information

Vertifree with NDC 68703-353 is a a human over the counter drug product labeled by Silver Star Brands. The generic name of Vertifree is bryonia, cocculus, gesemium, lobelia. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Silver Star Brands

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

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.

Vertifree 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.

  • LOBELIA INFLATA 30 [hp_C]/1801

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.

  • SUCROSE (UNII: C151H8M554)

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: Silver Star Brands
Labeler Code: 68703
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: 12-25-2020 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.

Vertifree 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

Hpus Active Ingredients

HPUS Active Ingredients: Each tablet contains equal parts of: Bryonia 30C, Cocculus 30C, Gelsemium 30C, Lobelia inf 30C.


Uses*: Homeopathic remedy for temporary relief of dizziness and nausea.*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.


Warnings: If symptoms persist or worsen, consult a healthcare professional. If pregnant or breastfeeding, ask a health professional before use. Keep this and all medication out ofreach of children. In an overdose, get medical help or contact an Poison Control Center right away.


Directions: Chew or dissolve tablet in the mouth. Alternatively, for small babies, crush tablets and sprinkle onto tongue or mix in warm water or soft food. For all ages: Acute: Take 2 tablets every 20 minutes or until symptoms subside. Chronic: Take 2 tables 3 times daily on an empty stomach.

Other Safety Information

Tamper resistant for your protection. Use only if seal is intact.Contains no artificial flavors or colorants. No gluten added. Lactose-free.

Inactive Ingredients:

Inactive Ingredients: Magnesium stearate, Maltodextrin, Sucrose.

Otc - Keep Out Of Reach Of Children

Keep this and all medication out of reach of children.

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, ask a health professional before use.

Otc - Purpose

Temporarily relieves dizziness & nausea**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

* Please review the disclaimer below.