NDC 43857-0290 Sinuforce

Echinacea (angustifolia), Hydrastis Canadensis, Nux Moschata, Trigonella Foenum Graecum, Arsenicum Album, Kali Bichromicum, Mercurius Sulphuratus Ruber, Pulsatilla (vulgaris), Sepia, Mercurius Solubilis

NDC Product Code 43857-0290

NDC 43857-0290-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Sinuforce with NDC 43857-0290 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Sinuforce is echinacea (angustifolia), hydrastis canadensis, nux moschata, trigonella foenum graecum, arsenicum album, kali bichromicum, mercurius sulphuratus ruber, pulsatilla (vulgaris), sepia, mercurius solubilis. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Bioactive Nutritional, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Sinuforce 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.

  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • GOLDENSEAL 3 [hp_X]/mL
  • NUTMEG 3 [hp_X]/mL
  • FENUGREEK SEED 3 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • POTASSIUM DICHROMATE 12 [hp_X]/mL
  • MERCURIC SULFIDE 12 [hp_X]/mL
  • PULSATILLA VULGARIS 12 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
  • MERCURIUS SOLUBILIS 30 [hp_X]/mL

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.

  • Oral - Administration to or by way of the mouth.
  • 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: Bioactive Nutritional, Inc.
Labeler Code: 43857
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: 03-21-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 11-18-2020 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Sinuforce Product Label Images

Sinuforce 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

Active Ingredients:

Echinacea (Angustifolia) 3X, Hydrastis canadensis 3X, Nux moschata 3X, Trigonella foenum graecum 3X, Arsenicum album 12X, Kali bichromicum 12X, Mercurius sulphuratus ruber 12X, Pulsatilla (vulgaris) 12x, Sepia 12X, Mercurius solubilis 30X.

Indications:

For temporary relief of allergic rhinitis with runny nose, nasal mucus with yellow-green discharge, pain and swelling of sinus cavities, and nasal drip.

For temporary relief of allergic rhinitis with runny nose, nasal mucus with yellow-green discharge, pain and swelling of sinus cavities, and nasal drip.

Warnings:

If pregnant or breast-feeding, ask a health care professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store in cool, dry place.

Keep Out Of Reach Of Children.

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized water, 25% Ethanol.

Questions:

Distributed by:BIOACTIVE NUTRITIONALMelbourne, FL 32935For Nutritional Information write:BioActive Nutritional, Inc.1803 N. Wickham Rd.Melbourne, FL 32935

Package Label Display:

BioActive HomeopathicSINUFORCE1 FL OZ (30 ml)

* Please review the disclaimer below.