NDC 55714-2365 Vitality

NDC Product Code 55714-2365

NDC 55714-2365-0

Package Description: 7.08 g in 1 BOTTLE, GLASS

NDC 55714-2365-1

Package Description: 28.35 g in 1 BOTTLE, GLASS

NDC 55714-2365-2

Package Description: 56.7 g in 1 BOTTLE, GLASS

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Vitality with NDC 55714-2365 is a product labeled by Newton Laboratories, Inc.. The generic name of Vitality is . The product's dosage form is and is administered via form.

Labeler Name: Newton Laboratories, Inc.

Dosage Form: -

Product Type: 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.

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)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Newton Laboratories, Inc.
Labeler Code: 55714
Start Marketing Date: 03-01-2011 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: I 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.

Vitality Product Label Images

Vitality 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

Indications & Usage Section

Vitality  Formulated for symptoms associated with low energy, mild stress and weakness.

Dosage & Administration Section

Directions:  Adults, take 6 pellets orally as needed or as directed by a healthcare professional. Sensitive persons begin with 1 pellet and gradually increase to full dose.

Otc - Active Ingredient Section

Adrenalinum 15x, Aloe 15x, Arsenicum alb. 15x, Baptisia 15x, Berber. aqui. 15x, Berber. vulg. 15x, Bryonia 15x, Chelidonium majus 15x, Crotalus horridus 15x, Digitalis 15x, Ferrum metallicum 15x, Glonoinum 15x, Glycyrrhiza glabra 15x, Hydrocotyle 15x, Iodium 15x, Iris versicolor 15x, Lachesis 15x, Lycopodium 15x, Nat. mur. 15x, Nux vom. 15x, Rhus toxicodendron 15x, Ruta 15x, Thuja occ. 15x, Thyroidinum 15x, Echinacea 3x, Lappa 3x, Solidago 3x, Taraxacum 3x.

Otc - Purpose Section

Formulated for symptoms associated with low energy, mild stress and weakness.

Inactive Ingredient Section

Inactive Ingredients: Gluten-free, non-GMO, beet-derived pellets.

Questions Section

Www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012Questions?  1.800.448.7256

Warnings Section

Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children

Otc - Pregnancy Or Breast Feeding Section

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children.

* Please review the disclaimer below.