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  4. NDC Product Code: 70942-811 Dr. Butler Hemorrhoid Treatment

NDC 70942-811 Dr. Butler Hemorrhoid Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70942-811?
  4. Dr. Butler Hemorrhoid Treatment Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70942-811
Proprietary Name:
Dr. Butler Hemorrhoid Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Beyond Health P.a.
Labeler Code:
70942
Product Label ID:
b5e5dc70-2708-6e16-e053-2a95a90ac204
Start Marketing Date: [9]
12-07-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 70942-811?

The NDC code 70942-811 is assigned by the FDA to the product Dr. Butler Hemorrhoid Treatment which is product labeled by Beyond Health P.a.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70942-811-03 85 g in 1 can . 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 Dr. Butler Hemorrhoid Treatment?

Temporarily reduces swelling associated with hemorrhoidal tissue. Temporary relief of anorectal itching and discomfort associated with hemorrhoids and other anorectal disorders.

Which are Dr. Butler Hemorrhoid Treatment UNII Codes?

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

Which are Dr. Butler Hemorrhoid Treatment 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:

What is the NDC to RxNorm Crosswalk for Dr. Butler Hemorrhoid Treatment?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1599785 - phenylephrine HCl 0.25 % / witch hazel 50 % Rectal Spray
  • RxCUI: 1599785 - phenylephrine hydrochloride 2.5 MG/ML / witch hazel 500 MG/ML Rectal Spray
  • RxCUI: 1599785 - phenylephrine hydrochloride 0.25 % / witch hazel 50 % Rectal Spray

* 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".