NDC Compounded Drug 5446-1476-01 Phenol

Solution Perineural

Compounded Drug Product Information

NDC Product Code 5446-1476
NDC Package Code 5446-1476-01
11-Digit NDC Billing Format NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
05446147601
Package Description 10 mL in 1 SYRINGE
Product Type What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Human Compounded Drug
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Phenol 6% Solution
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Phenol 6% Solution
Substance Name What is the Substance Name?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
Phenol
Dosage Form Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Route Name Perineural - Administration surrounding a nerve or nerves.
Marketing Category OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Code 5446
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Edge Pharma Llc
Substance Name Phenol
Active Ingredients Information 60 mg/1 mL
Reporting Period 2021-2

NDC Crossover Products Matching Phenol

NDC crossover of Phenol 6% Solution with NDC 5446-1476 a human compounded drug with other similar products matching the same substance name (Phenol) and the same administration route (perineural) or dosage form (solution).

Frequently Asked Questions

What is the NDC number assigned to Phenol 89% 3ml Bottle?

Phenol 89% 3ml Bottle was assigned by its manufacturer with NDC product code 5446-1476. This product is a drug classified as a human compounded drug. Compounded drugs are medications created by combining or altering existing drugs to meet the specific needs of certain patients. The NDC directory only includes information about compounded drugs from facilities that choose to assign NDC numbers to their products.

Which are the NDC package codes for Phenol 89% 3ml Bottle?

The NDC package code 5446-1476-01 was assigned to a 10 mL in 1 SYRINGE of phenol administered perineural via solution.

Who manufactures this product?

Phenol 89% 3ml Bottle is manufactured by an outsourced facility and labeled by Edge Pharma Llc. All compounded drugs included in the NDC directory are classified as "Outsourcing Facility Compounded Human Drug Product (Exempt from Approval Requirements)". Outsourcing facilities are a type of drug compounding facility regulated under Section 503B of the FD&C Act could be eligible for exemptions from drug registration if they meet all the conditions specified under Section 503B.

Which are the NDC crossover matchings for this product?

We found 1 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Edge Pharma LLC with NDC product codes 5446-1211-03.