NDC 76523-062 Massage Men Gel Max Power

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:
76523-062
Proprietary Name:
Massage Men Gel Max Power
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Valley Of The Sun Cosmetics Llc
Labeler Code:
76523
Start Marketing Date: [9]
07-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Shape:
ROUND (C48348)

Product Packages

NDC Code 76523-062-15

Package Description: 15 g in 1 BOTTLE, DISPENSING

Product Details

What is NDC 76523-062?

The NDC code 76523-062 is assigned by the FDA to the product Massage Men Gel Max Power which is product labeled by Valley Of The Sun Cosmetics Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76523-062-15 15 g in 1 bottle, dispensing . 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 Massage Men Gel Max Power?

Apply a small amount to the head and shaft of the penis before intercourse, or use as directed by a doctor. Wash product off after intercourse. use only on intact, non-inflamed skin allow gel to dry prior to intercourse not suitable for oral use use as directed, not more than four times per day

Which are Massage Men Gel Max Power UNII Codes?

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

Which are Massage Men Gel Max Power 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".