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  4. NDC Product Code: 75956-145 Male Desensitizer Pleasure Balm

NDC 75956-145 Male Desensitizer Pleasure Balm

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75956-145?
  4. Male Desensitizer Pleasure 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:
75956-145
Proprietary Name:
Male Desensitizer Pleasure Balm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kama Sutra
Labeler Code:
75956
Product Label ID:
e078b85b-7d49-4d59-9aa1-23055b9b0265
Start Marketing Date: [9]
02-14-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 75956-145?

The NDC code 75956-145 is assigned by the FDA to the product Male Desensitizer Pleasure Balm which is product labeled by Kama Sutra. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75956-145-02 1 tube in 1 box / 50 ml in 1 tube (75956-145-01). 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 Male Desensitizer Pleasure Balm?

Discontinue use and consult a doctor ifThis product used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical supervision.You or your partner develop a rash or irritation, such as burning or itching.

Which are Male Desensitizer Pleasure Balm UNII Codes?

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

Which are Male Desensitizer Pleasure 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:

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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".