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  4. NDC Product Code: 75956-147 Pleasure Balm Kama Sutra

NDC 75956-147 Pleasure Balm Kama Sutra

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75956-147?
  4. Pleasure Balm Kama Sutra 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:
75956-147
Proprietary Name:
Pleasure Balm Kama Sutra
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kama Sutra
Labeler Code:
75956
Product Label ID:
20ec6319-8380-4729-8f0d-0a6eb153b629
Start Marketing Date: [9]
09-12-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 75956-147?

The NDC code 75956-147 is assigned by the FDA to the product Pleasure Balm Kama Sutra 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 75956-147-01 50 ml in 1 tube . 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 Pleasure Balm Kama Sutra?

Discontinue use and consult a doctor ifThis product, used as directed does not provide reliefYou or your partner develops a rash or irritation, such as burning or itchingCondition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few daysThe following symptoms appear: weakness, confusion, headache, difficulty breathing and/or pale, gray or blue colored skin as these may be signs of methemoglobinemia

Which are Pleasure Balm Kama Sutra UNII Codes?

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

Which are Pleasure Balm Kama Sutra 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".