NDC 51393-5003 More Focus

Taraxacum Officinale Root, Verbena Hastata Top, Lactuca Virosa Leaf, Chamomile Flower Oil, Arabica Coffee Bean, And Scutellaria Lateriflora Whole

NDC Product Code 51393-5003

NDC CODE: 51393-5003

Proprietary Name: More Focus 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: Taraxacum Officinale Root, Verbena Hastata Top, Lactuca Virosa Leaf, Chamomile Flower Oil, Arabica Coffee Bean, And Scutellaria Lateriflora Whole 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

  • 51393 - Forces Of Nature

NDC 51393-5003-1

Package Description: 1 BOTTLE, DISPENSING in 1 CARTON > 10 mL in 1 BOTTLE, DISPENSING

NDC Product Information

More Focus with NDC 51393-5003 is a a human over the counter drug product labeled by Forces Of Nature. The generic name of More Focus is taraxacum officinale root, verbena hastata top, lactuca virosa leaf, chamomile flower oil, arabica coffee bean, and scutellaria lateriflora whole. The product's dosage form is solution/ drops and is administered via sublingual form.

Labeler Name: Forces Of Nature

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

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.

More Focus 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.

  • VERBENA HASTATA TOP 12 [hp_C]/100mL
  • LACTUCA VIROSA LEAF 12 [hp_C]/100mL
  • CHAMOMILE FLOWER OIL 30 [hp_C]/100mL
  • ARABICA COFFEE BEAN 30 [hp_C]/100mL

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.

  • Sublingual - Administration beneath the tongue.
  • Sublingual - Administration beneath the tongue.

Product Labeler Information

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

Labeler Name: Forces Of Nature
Labeler Code: 51393
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: 06-01-2020 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.

More Focus Product Label Images

More Focus 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


Drug Facts

Manufactured & Distributed by Forces of Nature, Inc. 21787 8th St East # 3A Sonoma, CA 95476 USA

Otc - Purpose

Active ingredientsPurposeTaraxacum officinaleUSDA Certified Organic 6CIrratibility, Impaired ThinkingVerbena 12CNervousness, Helps Brighten Mental PowersLactuca virosa 12CGreat Restlessness, Difficulty ConcentratingGerman chamomile 30CFor RestlessnessCoffea cruda 30CUnusual Mind Activity, Emotional AilmentsScutellaria lateriflora 12CFor Restlessness, Nervousness


To help focus mental abilities and restore calm thinking.


For oral (sublingual) use.

Otc - Ask Doctor

Ask a doctor before use in children under 3 years of age.

Otc - Stop Use

Stop use and ask doctor if symptoms persist for more than 3 days or worsen.

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding ask a doctor before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.


For all humans. Use as needed. For best results, use at the first sign of symptoms. Shake well before use.


Take 3-6 drops under the tongue.


Take 6-9 drops under the tongue.Repeat dosage 3-4 times per day when experiencing symptoms.

Other Information

  • Keep in cool dark place

Inactive Ingredients

Distilled Water, Grain Alcohol, Bergamot Oil

* Please review the disclaimer below.