NDC 43857-0440 Rheumaforce

Chondrus Crispus, Cimicifuga Racemosa, Spiraea Ulmaria, Trifolium Pratense, Urtica Urens, Xanthoxylum Fraxineum, Symphytum Officinale, Colchicum Autumnale, Ferrum Phosphoricum, Formica Rufa, Lithium Carbonicum, Natrum Sulphuricum, Rhododendron Chrysanthemum, Rhus Tox

NDC Product Code 43857-0440

NDC CODE: 43857-0440

Proprietary Name: Rheumaforce 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: Chondrus Crispus, Cimicifuga Racemosa, Spiraea Ulmaria, Trifolium Pratense, Urtica Urens, Xanthoxylum Fraxineum, Symphytum Officinale, Colchicum Autumnale, Ferrum Phosphoricum, Formica Rufa, Lithium Carbonicum, Natrum Sulphuricum, Rhododendron Chrysanthemum, Rhus Tox 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used to treat manic-depressive disorder (bipolar disorder). It works to stabilize the mood and reduce extremes in behavior by restoring the balance of certain natural substances (neurotransmitters) in the brain. Some of the benefits of continued use of this medication include decreasing how often manic episodes occur and decreasing the symptoms of manic episodes, such as exaggerated feelings of well-being, feelings that others wish to harm you, irritability, anxiousness, rapid/loud speech, and aggressive/hostile behaviors.

NDC Code Structure

  • 43857 - Bioactive Nutritional, Inc.

NDC 43857-0440-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Rheumaforce with NDC 43857-0440 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Rheumaforce is chondrus crispus, cimicifuga racemosa, spiraea ulmaria, trifolium pratense, urtica urens, xanthoxylum fraxineum, symphytum officinale, colchicum autumnale, ferrum phosphoricum, formica rufa, lithium carbonicum, natrum sulphuricum, rhododendron chrysanthemum, rhus tox. 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.

Rheumaforce 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.

  • CHONDRUS CRISPUS 3 [hp_X]/mL
  • BLACK COHOSH 3 [hp_X]/mL
  • FILIPENDULA ULMARIA ROOT 3 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
  • URTICA URENS 3 [hp_X]/mL
  • ZANTHOXYLUM AMERICANUM BARK 3 [hp_X]/mL
  • COMFREY ROOT 6 [hp_X]/mL
  • COLCHICUM AUTUMNALE BULB 12 [hp_X]/mL
  • FERROSOFERRIC PHOSPHATE 12 [hp_X]/mL
  • FORMICA RUFA 12 [hp_X]/mL
  • LITHIUM CARBONATE 12 [hp_X]/mL
  • SODIUM SULFATE 12 [hp_X]/mL
  • RHODODENDRON AUREUM LEAF 12 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 12 [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: 04-17-2017 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: 12-31-2020 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.

Rheumaforce Product Label Images

Rheumaforce 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

Inactive Ingredients:

Chondrus Crispus 3X, Cimicifuga Racemosa 3X, Spiraea Ulmaria 3X, Trifolium Pratense 3X, Urtica Urens 3X, Xanthoxylum Fraxineum 3X, Symphytum Officinale 6X, Colchicum Autumnale 12X, Ferrum Phosphoricum 12X, Formica Rufa 12X, Lithium Carbonicum 12X, Natrum Sulphuricum 12X, Rhododendron Chrysanthum 12X, Rhus Toxicodendron 12X.

Demineralized Water, 25% Ethanol.

Indications:

For temporary relief of pains throughout shoulder joint, arm, fingers, and small joints generally; swelling and tenderness of the finger and toe joints; and swellings in the joints with inflammation.

For temporary relief of pains throughout shoulder joint, arm, fingers, and small joints generally; swelling and tenderness of the finger and toe joints; and swellings in the joints with inflammation.

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.

Questions:

Distributed by:BioActive Nutritional, Inc.1803 N. Wickham Rd.Melbourne, FL 32935bioactivenutritional.com

Pakcage Label Display:

BIOActive NutritionalRHEUMAFORCEHOMEOPATHIC1 FL OZ (30 ml)

* Please review the disclaimer below.