NDC 72323-001 Medicated Oil

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72323-001
Proprietary Name:
Medicated Oil
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Luoyang Muchun Pharmaceutical Co, Ltd
Labeler Code:
72323
Start Marketing Date: [9]
06-15-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72323-001-30

Package Description: 1 BOTTLE, GLASS in 1 BOX / 10 mL in 1 BOTTLE, GLASS (72323-001-10)

Product Details

What is NDC 72323-001?

The NDC code 72323-001 is assigned by the FDA to the product Medicated Oil which is product labeled by Luoyang Muchun Pharmaceutical Co, Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72323-001-30 1 bottle, glass in 1 box / 10 ml in 1 bottle, glass (72323-001-10). 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 Medicated Oil?

Adults and children 12 years of age and older: Apply to the affected area 3 to 4 times daily. Children under 12 years of age:  Do not use, consult a doctor.

Which are Medicated Oil UNII Codes?

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

Which are Medicated 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 Medicated 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: 2048953 - menthol 8 % / methyl salicylate 26 % Topical Oil
  • RxCUI: 2048953 - menthol 80 MG/ML / methyl salicylate 260 MG/ML Topical Oil

* 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".