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  4. NDC Product Code: 10866-0090 Precaine B Chocolate Mint

NDC 10866-0090 Precaine B Chocolate Mint

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 10866-0090?
  5. Precaine B Chocolate Mint Uses
  6. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
10866-0090
Proprietary Name:
Precaine B Chocolate Mint
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pascal Company, Inc.
Labeler Code:
10866
Product Label ID:
5c63ebaf-c26b-2b92-e053-2991aa0a3a21
Start Marketing Date: [9]
08-16-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Flavor(s):
CHOCOLATE (C73376)
MINT (C73404)

Code Structure Chart

Product Details

What is NDC 10866-0090?

The NDC code 10866-0090 is assigned by the FDA to the product Precaine B Chocolate Mint which is product labeled by Pascal Company, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10866-0090-1 30 g in 1 jar . 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 Precaine B Chocolate Mint?

Application Directions:For topical use onlyFor best results apply to previously dried oral mucosa with cotton swab or similar applicator for adequate control of painRemoval of excess saliva during application minimizes dilution of the anesthetic and permits maximum penetrationNot more than 1.2 mg per Kg body weight per patient should be applied during a 24 hour period

Which are Precaine B Chocolate Mint UNII Codes?

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

* 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".