Pleasure Balm
NDC Package 75956-147-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Pleasure Balm is 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. Marketed by Kama Sutra, this product is identified by NDC 75956-147 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
75956-147-01
Package Description
50 mL in 1 TUBE
Product Code
75956-147
11-Digit Billing Format
75956014701

Clinical Specifications

Proprietary Name
Pleasure Balm Kama Sutra
Dosage Form
-
Usage Information
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

Regulatory & Marketing

Labeler Name
Kama Sutra
FDA Application #
part348
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
09-12-2013
Listing Expiration
12-31-2017
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 75956-147-01 identifies a specific commercial package of 50 ml in 1 tube of Pleasure Balm Kama Sutra, labeled by Kama Sutra. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Kama Sutra on September 12, 2013. The current certification is valid through December 31, 2017.

How is this Kama Sutra product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 75956014701. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
75956-147-01
11-Digit CMS (5-4-2)
75956-0147-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.