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  4. NDC Product Code: 59779-398 Dibucaine

NDC 59779-398 Dibucaine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59779-398?
  4. Dibucaine Uses
  5. Active Ingredients UNII Codes
  6. Inactive 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:
59779-398
Proprietary Name:
Dibucaine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Pharmacy
Labeler Code:
59779
Product Label ID:
e3807a1b-c375-456a-bd7e-de3a1607c8fc
Start Marketing Date: [9]
07-16-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59779-398-03

Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE

Product Details

What is NDC 59779-398?

The NDC code 59779-398 is assigned by the FDA to the product Dibucaine which is product labeled by Cvs Pharmacy. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59779-398-03 1 tube in 1 carton / 28 g in 1 tube. 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 Dibucaine?

Uses temporarily relieves pain and itching due to: - hemorrhoids or other anorectal disorders - sunburn - minor burns - minor cuts - scrapes - insect bites - minor skin irritation  Other information- to secure child resistant cap; screw cap tightly. Then turn cap in opposite direction.If clicking sound is not heard, repeat procedure.- see crimp of tube for lot number and expiration date-store at controlled room temperature 20 degrees to 25 degrees c (68 degrees to 77 degrees F)

Which are Dibucaine UNII Codes?

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

Which are Dibucaine 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:

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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".