NDC 43857-0598 Respiforce I Plus

Bryonia (alba), Eupatorium Perfoliatum, Ferrum Phosphoricum, Gelsemium Sempervirens, Kreosotum, Veratrum Viride, Anas Barbariae, Hepatis Et Cordis Extractum

NDC Product Code 43857-0598

NDC CODE: 43857-0598

Proprietary Name: Respiforce I Plus 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: Bryonia (alba), Eupatorium Perfoliatum, Ferrum Phosphoricum, Gelsemium Sempervirens, Kreosotum, Veratrum Viride, Anas Barbariae, Hepatis Et Cordis Extractum 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

  • 43857 - Bioactive Nutritional, Inc.

NDC 43857-0598-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Respiforce I Plus with NDC 43857-0598 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Respiforce I Plus is bryonia (alba), eupatorium perfoliatum, ferrum phosphoricum, gelsemium sempervirens, kreosotum, veratrum viride, anas barbariae, hepatis et cordis extractum. 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.

Respiforce I Plus 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.

  • BRYONIA ALBA ROOT 30 [hp_C]/mL
  • EUPATORIUM PERFOLIATUM FLOWERING TOP 30 [hp_C]/mL
  • FERROSOFERRIC PHOSPHATE 30 [hp_C]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 30 [hp_C]/mL
  • WOOD CREOSOTE 30 [hp_C]/mL
  • VERATRUM VIRIDE ROOT 30 [hp_C]/mL
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 30 [hp_C]/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.

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: 05-24-2021 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: 12-31-2022 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 - NO 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".

* Please review the disclaimer below.

Respiforce I Plus Product Label Images

Respiforce I Plus 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:

Bryonia (Alba) 30C, Eupatorium Perfoliatum 30C, Ferrum Phosphoricum 30C, Gelsemium Sempervirens 30C, Kreosotum 30C, Veratrum Viride 30C, Anas Barbariae, Hepatis ET Cordis Extractum 30C, 200C.

Indications:

For temporary relief of flu symptoms, fever, chills, body aches and pains.

For temporary relief of flu symptoms, fever, chills, body aches and pains.

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 Nutritional, Inc.1803 N. Wickham Rd.Melbourne, FL 32935bioactivenutritional.com

Package Label Display:

BIOActive NutritionalRESPIFORCE I PLUSHOMEOPATHIC1 FL OZ (30 ml)

* Please review the disclaimer below.