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  4. NDC Product Code: 71635-100 Mulbit Me Firming Sleeping Pack

NDC 71635-100 Mulbit Me Firming Sleeping Pack

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71635-100?
  4. Mulbit Me Firming Sleeping 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:
71635-100
Proprietary Name:
Mulbit Me Firming Sleeping 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:
4d348bbf-cd88-432d-8f1a-b9f484ce6d52
Start Marketing Date: [9]
10-01-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71635-100-02

Package Description: 1 TUBE in 1 CARTON / 50 mL in 1 TUBE (71635-100-01)

Product Details

What is NDC 71635-100?

The NDC code 71635-100 is assigned by the FDA to the product Mulbit Me Firming Sleeping 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 71635-100-02 1 tube in 1 carton / 50 ml in 1 tube (71635-100-01). 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 Mulbit Me Firming Sleeping Pack?

Directions: Apply an adequate amount to all over the face at night and sleep with the product on the face.

Which are Mulbit Me Firming Sleeping Pack UNII Codes?

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

Which are Mulbit Me Firming Sleeping 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".