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  4. NDC Product Code: 27293-033 Budpak Petroleum

NDC 27293-033 Budpak Petroleum

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 27293-033?
  4. Budpak Petroleum Uses
  5. Active Ingredients UNII Codes
  6. 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:
27293-033
Proprietary Name:
Budpak Petroleum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Budpak Inc.
Labeler Code:
27293
Product Label ID:
df33b4b5-e4ce-476c-a151-fc81ce266c1a
Start Marketing Date: [9]
07-07-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 27293-033?

The NDC code 27293-033 is assigned by the FDA to the product Budpak Petroleum which is product labeled by Budpak Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 27293-033-06 113 g in 1 bottle , 27293-033-07 283 g in 1 bottle , 27293-033-11 368 g in 1 bottle , 27293-033-12 226 g in 1 bottle , 27293-033-13 170 g in 1 bottle . 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 Budpak Petroleum?

UsesTemporarily protects minor cuts, scrapes or burns.Temporarily protects and helps relieve chapped or cracked skin and lips.Helps protect from the drying effects of wind and cold weather.

Which are Budpak Petroleum UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Budpak Petroleum?

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:

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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".