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NDC 69384-070 Msm Scalp Essence Signature

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69384-070?
  4. Msm Scalp Essence Signature Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69384-070
Proprietary Name:
Msm Scalp Essence Signature
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hairjoy
Labeler Code:
69384
Product Label ID:
1d4025c5-8f8b-4a32-b044-b5dec8b1b2f9
Start Marketing Date: [9]
08-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 69384-070?

The NDC code 69384-070 is assigned by the FDA to the product Msm Scalp Essence Signature which is product labeled by Hairjoy. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69384-070-02 1 container in 1 carton / 120 ml in 1 container (69384-070-01). 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 Msm Scalp Essence Signature?

■Use it after shampooing. Use your scalp after drying it.

Which are Msm Scalp Essence Signature UNII Codes?

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

Which are Msm Scalp Essence Signature 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:

What is the NDC to RxNorm Crosswalk for Msm Scalp Essence Signature?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* 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".