NDC 0362-9023 Octocaine 100

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:
0362-9023
Proprietary Name:
Octocaine 100
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Septodont
Labeler Code:
0362
Start Marketing Date: [9]
11-07-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 0362-9023-05

Package Description: 50 CARTRIDGE in 1 CARTON / 1.7 mL in 1 CARTRIDGE

Product Details

What is NDC 0362-9023?

The NDC code 0362-9023 is assigned by the FDA to the product Octocaine 100 which is product labeled by Septodont. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0362-9023-05 50 cartridge in 1 carton / 1.7 ml in 1 cartridge. 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 Octocaine 100?

Octocaine (Lidocaine and Epinephrine Injection, USP) is indicated for the production of local anesthesia for dental procedures by nerve block or infiltration techniques.Only accepted procedures for these techniques as described in standard textbooks are recommended.

Which are Octocaine 100 UNII Codes?

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

Which are Octocaine 100 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 Octocaine 100?

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: 1011820 - Octocaine 100 2 % with EPINEPHrine 1:100,000 in 1.7 mL Dental Cartridge
  • RxCUI: 1011820 - 1.7 ML epinephrine 0.01 MG/ML / lidocaine hydrochloride 20 MG/ML Cartridge [Octocaine with Epinephrine]
  • RxCUI: 1011820 - Octocaine 2 % with epinephrine 1:100,000 1.7 ML Dental Cartridge
  • RxCUI: 1293648 - lidocaine HCl 2 % / EPINEPHrine 1:100,000 in 1.7 mL Dental Cartridge
  • RxCUI: 1293648 - 1.7 ML epinephrine 0.01 MG/ML / lidocaine hydrochloride 20 MG/ML Cartridge

* 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".