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  4. NDC Product Code: 50730-1481 Cocoa Butter, Phenylephrine Hydrochloride, Shark Liver Oil

NDC 50730-1481 Cocoa Butter, Phenylephrine Hydrochloride, Shark Liver Oil

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50730-1481?
  4. Cocoa Butter, Phenylephrine Hydrochloride, Shark Liver Oil 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:
50730-1481
Proprietary Name:
Cocoa Butter, Phenylephrine Hydrochloride, Shark Liver Oil
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
H And P Industries, Inc. Dba Triad Group
Labeler Code:
50730
Product Label ID:
e56eb547-9a1f-4f37-a0f6-95b3c1f27e65
Start Marketing Date: [9]
03-06-2004
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50730-1481-1

Package Description: 12 SUPPOSITORY in 1 BOX

Product Details

What is NDC 50730-1481?

The NDC code 50730-1481 is assigned by the FDA to the product Cocoa Butter, Phenylephrine Hydrochloride, Shark Liver Oil which is product labeled by H And P Industries, Inc. Dba Triad Group. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50730-1481-1 12 suppository in 1 box . 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 Cocoa Butter, Phenylephrine Hydrochloride, Shark Liver Oil?

Adults:When practical, cleanse the affected area by patting or blotting with an appropriate cleansing tissue. Gently dry by patting or blotting with toilet tissue or soft cloth before insertion of this product.Detach one suppository from stripRemove wrapper before inserting into rectumHold suppository with rounded end up and insert tip of fingernail at end marked "peel down"Carefully peel film slowly and evenly down both sides to expose suppositoryInsert one suppository into rectum up to 4 times daily especially at night and morning or after each bowel movementChildren under 12 years:  ask a doctor

Which are Cocoa Butter, Phenylephrine Hydrochloride, Shark Liver Oil UNII Codes?

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

Which are Cocoa Butter, Phenylephrine Hydrochloride, Shark Liver Oil 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 Cocoa Butter, Phenylephrine Hydrochloride, Shark Liver Oil?

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: 259093 - cocoa butter 85.5 % / phenylephrine HCl 0.25 % / shark liver oil 3 % Rectal Suppository
  • RxCUI: 259093 - cocoa butter 0.855 MG/MG / phenylephrine 0.0025 MG/MG / shark liver oil 0.03 MG/MG Rectal Suppository
  • RxCUI: 259093 - cocoa butter 85.5 % / phenylephrine 0.25 % / shark liver oil preparation 3 % 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".