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  4. NDC Product Code: 50730-4536 Mineral Oil, Petrolatum, Phenylephrine Hydrochloride, Shark Liver Oil

NDC 50730-4536 Mineral Oil, Petrolatum, Phenylephrine Hydrochloride, Shark Liver Oil

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50730-4536?
  4. Mineral Oil, Petrolatum, 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:
50730-4536
Proprietary Name:
Mineral Oil, Petrolatum, 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:
30d26837-57e4-476c-9f5b-0171746fad2c
Start Marketing Date: [9]
07-01-2005
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50730-4536-0

Package Description: 1 TUBE, WITH APPLICATOR in 1 BOX / 56.7 g in 1 TUBE, WITH APPLICATOR

Product Details

What is NDC 50730-4536?

The NDC code 50730-4536 is assigned by the FDA to the product Mineral Oil, Petrolatum, 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 50730-4536-0 1 tube, with applicator in 1 box / 56.7 g in 1 tube, with applicator. 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 Mineral Oil, Petrolatum, 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 application of this ointment.Apply to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movement.For intrarectal use:Before applying, remove protective cover from applicator. Attach applicator to tube. Lubricate applicator well and then gently insert applicator into the rectum. Thoroughly clean applicator after each use and replace protective cover.Also apply ointment to external area.Children under 12 years:  ask a doctor.

Which are Mineral Oil, Petrolatum, Phenylephrine Hydrochloride, Shark Liver Oil UNII Codes?

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

Which are Mineral Oil, Petrolatum, 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 Mineral Oil, Petrolatum, 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: 1544968 - mineral oil 14 % / petrolatum 71.9 % / phenylephrine HCl 0.25 % / shark liver oil preparation 3 % Rectal Ointment
  • RxCUI: 1544968 - mineral oil 0.14 MG/MG / petrolatum 0.719 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG / shark liver oil 0.03 MG/MG Rectal Ointment

* 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".