NDC 51393-5002 Sinus Maximum Strength

Holy Basil Leaf, Berberis Vulgaris Root, Garlic, Thuja Occidentalis Leaf, Echinacea Angustifolia Root, And Silicon Dioxide

NDC Product Code 51393-5002

NDC CODE: 51393-5002

Proprietary Name: Sinus Maximum Strength 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: Holy Basil Leaf, Berberis Vulgaris Root, Garlic, Thuja Occidentalis Leaf, Echinacea Angustifolia Root, And Silicon Dioxide 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

NDC 51393-5002-1

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

NDC Product Information

Sinus Maximum Strength with NDC 51393-5002 is a a human over the counter drug product labeled by Forces Of Nature. The generic name of Sinus Maximum Strength is holy basil leaf, berberis vulgaris root, garlic, thuja occidentalis leaf, echinacea angustifolia root, and silicon dioxide. 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.

Sinus Maximum Strength 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.

  • HOLY BASIL LEAF 89 [hp_C]/100mL
  • GARLIC 89 [hp_C]/100mL
  • SILICON DIOXIDE 55 [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.

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: 02-01-2019 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.

Sinus Maximum Strength Product Label Images

Sinus Maximum Strength 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 byFORCES OF NATURE®21787 8th St East #3A Sonoma, CA 95476 USA

Otc - Purpose

Active ingredientsOcimumUSDA Certified Organic 89CHelps Clear CongestionBerberis vulgaris 34CTo Clear MucusAllium sativum 89CClears Runny NoseThuja occidentalis 89CTo Clear Sinus MucusEchinacea angustifolia 55CRelieves Stuffy NoseSilica 55CRelief for Itchy NoseTrigonella foenum-graecum 89CExpectorant, for Flu-Like Symptoms


  • For the relief of sinus related ailments. Symptoms include:Nasal CongestionSinus PressureItchy/Runny Nose


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.


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

For Sinus Issues

Take 5-10 drops under the tongue.If symptoms persist, repeat dose under the tongue (5-10) drops approximately 4-5 times per day until symptoms subside.

Other Information

  • Store in a cool dark place

Inactive Ingredients

Distilled Water, Grain Alcohol

* Please review the disclaimer below.