NDC Compounded Drug 73271-6142-1 Prilocaine; Lidocaine; Tetracaine; Phenylephrine

Gel Dental

Table of Contents

    1. Compounded Product Information
    2. NDC Crossover Products Matching Lidocain/prilocain/tetracain/phenylephrine 10/10/4/2% 30gm Mint Flavor
    3. Frequently Asked Questions

Compounded Drug Product Information

NDC Product Code 73271-6142
NDC Package Code 73271-6142-1
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.		 73271614201
Package Description 1 GEL in 1 JAR
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.		 Lidocain/prilocain/tetracain/phenylephrine 10/10/4/2% 30gm Mint Flavor
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.		 Lidocain/prilocain/tetracain/phenylephrine 10/10/4/2% 30gm Mint Flavor
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.		 Prilocaine; Lidocaine; Tetracaine; Phenylephrine
Dosage Form Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Route Name Dental - Administration to a tooth or teeth.
Marketing Category OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Code 73271
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		 Right Value Drug Stores Llc Dba Carie Boyd's Prescription Shop
Substance Name Prilocaine; Lidocaine; Tetracaine; Phenylephrine
Active Ingredients Information 3 g; 3 g; 1.2 g; .6 g
Reporting Period 2021-2

NDC Crossover Products Matching Prilocaine; Lidocaine; Tetracaine; Phenylephrine

NDC crossover of Lidocain/prilocain/tetracain/phenylephrine 10/10/4/2% 30gm Mint Flavor with NDC 73271-6142 a human compounded drug with other similar products matching the same substance name (Prilocaine; Lidocaine; Tetracaine; Phenylephrine) and the same administration route (dental) or dosage form (gel).

Frequently Asked Questions

What is the NDC number assigned to Lidocain/prilocain/tetracain/phenylephrine 10/10/4/2% 30gm Tuttifrutti Flavor?

Lidocain/prilocain/tetracain/phenylephrine 10/10/4/2% 30gm Tuttifrutti Flavor was assigned by its manufacturer with NDC product code 73271-6142. 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 Lidocain/prilocain/tetracain/phenylephrine 10/10/4/2% 30gm Tuttifrutti Flavor?

The NDC package code 73271-6142-1 was assigned to a 1 GEL in 1 JAR of prilocaine; lidocaine; tetracaine; phenylephrine administered dental via gel.

Who manufactures this product?

Lidocain/prilocain/tetracain/phenylephrine 10/10/4/2% 30gm Tuttifrutti Flavor is manufactured by an outsourced facility and labeled by Right Value Drug Stores Llc Dba Carie Boyd's Prescription Shop. 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 3 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Right Value Drug Stores llc dba Carie Boyd's Prescription Shop with NDC product codes 73271-7142-1, 73271-8142-1 and 73271-9142-1.