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  4. NDC Product Code: 61357-135 Hemorrodil

NDC 61357-135 Hemorrodil

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 61357-135?
  4. Hemorrodil 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:
61357-135
Proprietary Name:
Hemorrodil
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zurich Medical Labs, Llc
Labeler Code:
61357
Product Label ID:
1c704359-89a4-449c-961c-ad527cb467c2
Start Marketing Date: [9]
03-01-1964
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61357-135-01

Package Description: 1 BLISTER PACK in 1 CARTON / 12 SUPPOSITORY in 1 BLISTER PACK

Product Details

What is NDC 61357-135?

The NDC code 61357-135 is assigned by the FDA to the product Hemorrodil which is product labeled by Zurich Medical Labs, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61357-135-01 1 blister pack in 1 carton / 12 suppository in 1 blister pack. 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 Hemorrodil?

This product is used as Active IngredientsPurposePhenylephrine Hydrochloride 0.25%VasoconstrictorCocoa Butter 88.44%Protectant. Temporarily shrinks hemorrhoidal tissuesProvides temporary relief from the itching, burning and discomfort associated with hemorrhoidsAids in protecting irritated anorectal areas

Which are Hemorrodil UNII Codes?

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

Which are Hemorrodil 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 Hemorrodil?

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: 1438497 - cocoa butter 88.4 % / phenylephrine HCl 0.25 % Rectal Suppository
  • RxCUI: 1438497 - cocoa butter 0.884 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Suppository
  • RxCUI: 1491717 - Hemorrodil 88.44 % / 0.25 % Rectal Suppository
  • RxCUI: 1491717 - cocoa butter 0.884 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Suppository [Hemorrodil]
  • RxCUI: 1491717 - Hemorrodil (cocoa butter 88.44 % / phenylephrine HCl 0.25 % ) Rectal Suppository

* 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".