NDC 10705-077 Mandelay Male Genital Desensitizer

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:
10705-077
Proprietary Name:
Mandelay Male Genital Desensitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Majestic Drug Co., Inc.
Labeler Code:
10705
Start Marketing Date: [9]
10-31-1995
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 10705-077-01

Package Description: 1 TUBE in 1 BOX / 28.35 g in 1 TUBE (10705-077-28)

Product Details

What is NDC 10705-077?

The NDC code 10705-077 is assigned by the FDA to the product Mandelay Male Genital Desensitizer which is product labeled by Majestic Drug Co., Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10705-077-01 1 tube in 1 box / 28.35 g in 1 tube (10705-077-28). 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 Mandelay Male Genital Desensitizer?

Apply a small amount to head and shaft of penis 2-3 minutes before intercourse, or use as directed by a physician.Wash product off after intercourse.

Which are Mandelay Male Genital Desensitizer UNII Codes?

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

Which are Mandelay Male Genital Desensitizer 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:

  • CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)

* 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".