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  4. NDC Product Code: 59985-105 Remedi Health Solutions Calendula Cream

NDC 59985-105 Remedi Health Solutions Calendula Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59985-105?
  4. Remedi Health Solutions Calendula Cream 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:
59985-105
Proprietary Name:
Remedi Health Solutions Calendula Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chc Montana
Labeler Code:
59985
Product Label ID:
85dbb272-e0ab-4a20-86e0-7e473d0e549d
Start Marketing Date: [9]
01-01-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 59985-105?

The NDC code 59985-105 is assigned by the FDA to the product Remedi Health Solutions Calendula Cream 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 59985-105-12 1 jar in 1 box / 28 g in 1 jar. 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 Calendula Cream?

Apply to sore or irritated area including skin, mouth, lips, genitals. Apply 2 times daily. May be used additionally for comfort for up to 7 days.May be applied to the wrist for internal healing benefits.

Which are Remedi Health Solutions Calendula Cream UNII Codes?

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

  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)

Which are Remedi Health Solutions Calendula Cream 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".