NDC 69626-0049 Tanac Oral Pain Reliever

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:
69626-0049
Proprietary Name:
Tanac Oral Pain Reliever
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Leosons Overseas Corp
Labeler Code:
69626
Start Marketing Date: [9]
01-01-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69626-0049-4

Package Description: 1 BOTTLE in 1 CARTON / 13.3 mL in 1 BOTTLE

Product Details

What is NDC 69626-0049?

The NDC code 69626-0049 is assigned by the FDA to the product Tanac Oral Pain Reliever which is product labeled by Leosons Overseas Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69626-0049-4 1 bottle in 1 carton / 13.3 ml in 1 bottle. 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 Tanac Oral Pain Reliever?

Apply product with cotton swab or clean fingertip to the affected areaadults and children 2 years of age and older: use up times 4 times daily or as directed by a dentist or doctor. Children should be supervised in the use of this product.children under 2 years of age: do not use

Which are Tanac Oral Pain Reliever UNII Codes?

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

Which are Tanac Oral Pain Reliever 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 Tanac Oral Pain Reliever?

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: 1053339 - Tanac Liquid 10 % Mucous Membrane Topical Solution
  • RxCUI: 1053339 - benzocaine 100 MG/ML Mucous Membrane Topical Solution [Tanac Liquid]
  • RxCUI: 1053339 - Tanac Liquid 100 MG/ML Mucous Membrane Topical Solution
  • RxCUI: 583152 - benzocaine 10 % Mucous Membrane Topical Solution
  • RxCUI: 583152 - benzocaine 100 MG/ML Mucous Membrane Topical Solution

* 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".