1. Home
  2. Labeler Index
  3. W Sternoff Llc
  4. NDC Product Code: 15197-007 Bodyglide Anti Chafe Balm

NDC 15197-007 Bodyglide Anti Chafe Balm

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 15197-007?
  4. Bodyglide Anti Chafe Balm 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:
15197-007
Proprietary Name:
Bodyglide Anti Chafe Balm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
W Sternoff Llc
Labeler Code:
15197
Product Label ID:
05bac498-5d1b-4329-9c06-0cc59f9c8d8e
Start Marketing Date: [9]
11-24-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 15197-007?

The NDC code 15197-007 is assigned by the FDA to the product Bodyglide Anti Chafe Balm which is product labeled by W Sternoff Llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 15197-007-07 2 g in 1 tube , 15197-007-14 1 tube in 1 package / 36.9 g in 1 tube (15197-007-13), 15197-007-26 1 tube in 1 package / 70 g in 1 tube (15197-007-25), 15197-007-46 1 tube in 1 package / 12.8 g in 1 tube (15197-007-45). 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 Bodyglide Anti Chafe Balm?

Apply as needed.

Which are Bodyglide Anti Chafe Balm UNII Codes?

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

Which are Bodyglide Anti Chafe Balm 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".