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  4. NDC Product Code: 59985-323 Remedi Health Solutions Diminish Gluten Reactivity

NDC 59985-323 Remedi Health Solutions Diminish Gluten Reactivity

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59985-323?
  4. Remedi Health Solutions Diminish Gluten Reactivity 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:
59985-323
Proprietary Name:
Remedi Health Solutions Diminish Gluten Reactivity
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chc Montana
Labeler Code:
59985
Product Label ID:
917e786a-f4ac-485c-9e80-585a5b3b14fa
Start Marketing Date: [9]
01-01-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 59985-323?

The NDC code 59985-323 is assigned by the FDA to the product Remedi Health Solutions Diminish Gluten Reactivity which is product labeled by Chc Montana. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59985-323-32 1 bottle, spray in 1 box / 30 ml in 1 bottle, spray. 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 Remedi Health Solutions Diminish Gluten Reactivity?

Repeat 1 oral spray 3 times in a row, separated 5 minutes apart.May be repeated 3 additional times or as needed.May also be taken ahead of a meal or snack.

Which are Remedi Health Solutions Diminish Gluten Reactivity UNII Codes?

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

  • CHRYSOPOGON ZIZANIOIDES ROOT (UNII: 37TB8LUP9Z)
  • CHRYSOPOGON ZIZANIOIDES ROOT (UNII: 37TB8LUP9Z) (Active Moiety)
  • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
  • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8)
  • DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8) (Active Moiety)
  • OKOUBAKA AUBREVILLEI BARK (UNII: MK2074187Z)
  • OKOUBAKA AUBREVILLEI BARK (UNII: MK2074187Z) (Active Moiety)

Which are Remedi Health Solutions Diminish Gluten Reactivity 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:

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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".