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  4. NDC Product Code: 43857-0598 Respiforce I Plus

NDC 43857-0598 Respiforce I Plus

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0598?
  4. Respiforce I Plus Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
43857-0598
Proprietary Name:
Respiforce I Plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bioactive Nutritional, Inc.
Labeler Code:
43857
Product Label ID:
3da3fc7e-eb9c-4cd3-95ee-3250dd90c9c7
Start Marketing Date: [9]
05-24-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 43857-0598?

The NDC code 43857-0598 is assigned by the FDA to the product Respiforce I Plus which is product labeled by Bioactive Nutritional, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43857-0598-1 30 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Respiforce I Plus?

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

Which are Respiforce I Plus UNII Codes?

The UNII codes for the active ingredients in this product are:

  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
  • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
  • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • WOOD CREOSOTE (UNII: 3JYG22FD73)
  • WOOD CREOSOTE (UNII: 3JYG22FD73) (Active Moiety)
  • VERATRUM VIRIDE ROOT (UNII: 197B3Q7T5Q)
  • VERATRUM VIRIDE ROOT (UNII: 197B3Q7T5Q) (Active Moiety)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)

Which are Respiforce I Plus 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:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[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".