NDC 66096-397 Vida Hair

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:
66096-397
Proprietary Name:
Vida Hair
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ohm Pharma Inc.
Labeler Code:
66096
Start Marketing Date: [9]
01-02-2017
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 66096-397-07

Package Description: 120 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 66096-397?

The NDC code 66096-397 is assigned by the FDA to the product Vida Hair which is product labeled by Ohm Pharma Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66096-397-07 120 ml in 1 bottle, plastic . 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.

Which are Vida Hair UNII Codes?

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

  • ARNICA MONTANA (UNII: O80TY208ZW)
  • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
  • ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79)
  • ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79) (Active Moiety)

Which are Vida Hair 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".