NDC 51393-5002 Sinus Maximum Strength
Holy Basil Leaf,Berberis Vulgaris Root,Garlic,Thuja Occidentalis Leaf,Echinacea - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51393 - Forces Of Nature
- 51393-5002 - Sinus
Product Packages
NDC Code 51393-5002-1
Package Description: 1 BOTTLE, DISPENSING in 1 CARTON / 10 mL in 1 BOTTLE, DISPENSING
NDC Code 51393-5002-3
Package Description: 1 BOTTLE, DISPENSING in 1 CARTON / 30 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 51393-5002?
What are the uses for Sinus Maximum Strength?
What are Sinus Maximum Strength Active Ingredients?
- BERBERIS VULGARIS ROOT 34 [hp_C]/100mL
- ECHINACEA ANGUSTIFOLIA ROOT 55 [hp_C]/100mL
- GARLIC 89 [hp_C]/100mL - A species of Allium used as a spice (SPICES) and traditional remedy. It contains alliin lyase and alliin, which is converted by alliin lyase to allicin, the pungent ingredient responsible for the aroma of fresh cut garlic.
- HOLY BASIL LEAF 89 [hp_C]/100mL
- SILICON DIOXIDE 55 [hp_C]/100mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- THUJA OCCIDENTALIS LEAF 89 [hp_C]/100mL
Which are Sinus Maximum Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOLY BASIL LEAF (UNII: SCJ765569P)
- HOLY BASIL LEAF (UNII: SCJ765569P) (Active Moiety)
- BERBERIS VULGARIS ROOT (UNII: ITJ40JX79U)
- BERBERIS VULGARIS ROOT (UNII: ITJ40JX79U) (Active Moiety)
- GARLIC (UNII: V1V998DC17)
- GARLIC (UNII: V1V998DC17) (Active Moiety)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA ROOT (UNII: D982V7VT3P)
- ECHINACEA ANGUSTIFOLIA ROOT (UNII: D982V7VT3P) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Sinus Maximum Strength Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Sinus Maximum Strength?
* Please review the disclaimer below.
[1] 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.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] 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.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".