NDC 51815-208 Right Guard Sport Active

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:
51815-208
Proprietary Name:
Right Guard Sport Active
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vvf Illinois Services Llc
Labeler Code:
51815
Start Marketing Date: [9]
12-01-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51815-208-01

Package Description: 51 g in 1 APPLICATOR

Product Details

What is NDC 51815-208?

The NDC code 51815-208 is assigned by the FDA to the product Right Guard Sport Active which is product labeled by Vvf Illinois Services Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51815-208-01 51 g in 1 applicator . 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 Right Guard Sport Active?

Apply to underarms only Apply to underarms only

Which are Right Guard Sport Active UNII Codes?

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

  • ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH)
  • ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH) (Active Moiety)

Which are Right Guard Sport Active 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:

* 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".