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  4. NDC Product Code: 71635-060 Man Power Pack

NDC 71635-060 Man Power Pack

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71635-060?
  4. Man Power Pack 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:
71635-060
Proprietary Name:
Man Power Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
First Cosmetic Co., Ltd
Labeler Code:
71635
Product Label ID:
92c793a4-a3c5-4cea-a907-74e49b4ced7b
Start Marketing Date: [9]
10-01-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 71635-060?

The NDC code 71635-060 is assigned by the FDA to the product Man Power Pack which is product labeled by First Cosmetic Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71635-060-02 10 pouch in 1 carton / 17 g in 1 pouch (71635-060-01). 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 Man Power Pack?

Directions:Massage Sheet for Prostate 1. Before opening, tap on the sheet 2~3times to evenly blend the essence. 2. Unfold the sheet and put it over the cleanly washed penis. 3. Pull the sheet down to cover the entire part.Massage Sheet for Glans 1. Take out the sheet for glans, unfold it in the middle and apply the essence to the sheet. 2. Dab the sheet thoroughly to let the sheet soak in the essence. 3. Unfold the soaked sheet completely and put it over the glans.

Which are Man Power Pack UNII Codes?

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

Which are Man Power Pack 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".