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  4. NDC Product Code: 70488-0003 J9 Ultra Advanced Intensive Recovery

NDC 70488-0003 J9 Ultra Advanced Intensive Recovery

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70488-0003?
  4. J9 Ultra Advanced Intensive Recovery 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:
70488-0003
Proprietary Name:
J9 Ultra Advanced Intensive Recovery
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Musee Cosmetic Co.,ltd.
Labeler Code:
70488
Product Label ID:
2c6b521a-72c6-42f8-e054-00144ff88e88
Start Marketing Date: [9]
02-22-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70488-0003-1

Package Description: 250 mL in 1 BOTTLE

Product Details

What is NDC 70488-0003?

The NDC code 70488-0003 is assigned by the FDA to the product J9 Ultra Advanced Intensive Recovery which is product labeled by Musee Cosmetic Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70488-0003-1 250 ml in 1 bottle . 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 J9 Ultra Advanced Intensive Recovery?

1) Moisten hair and scalp with warm water sufficiently 2) Apply a proper amount to foam and apply to the hair and scalp sufficiently. 3) Massage for about 5 minutes and rinse it.

Which are J9 Ultra Advanced Intensive Recovery UNII Codes?

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

Which are J9 Ultra Advanced Intensive Recovery 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".