NDC 51879-240 Tecnu Bites And Stings

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:
51879-240
Proprietary Name:
Tecnu Bites And Stings
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tec Laboratories, Inc.
Labeler Code:
51879
Start Marketing Date: [9]
02-03-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51879-240-20

Package Description: 1 PACKET in 1 CARTON / 20 CLOTH in 1 PACKET (51879-240-01)

Product Details

What is NDC 51879-240?

The NDC code 51879-240 is assigned by the FDA to the product Tecnu Bites And Stings which is product labeled by Tec Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51879-240-20 1 packet in 1 carton / 20 cloth in 1 packet (51879-240-01). 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 Tecnu Bites And Stings?

Uses:​• temporarily relieves the pain and itching of hot,burning, irritated, or inflamed skin due to:• minor insect bites and stings• promotes healing to help prevent scar tissue formation

Which are Tecnu Bites And Stings UNII Codes?

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

  • GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI)
  • GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (Active Moiety)
  • PLANTAGO MAJOR (UNII: W2469WNO6U)
  • PLANTAGO MAJOR (UNII: W2469WNO6U) (Active Moiety)
  • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
  • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) (Active Moiety)

Which are Tecnu Bites And Stings 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".