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  4. NDC Product Code: 58962-004 Vamousse Lice Protection

NDC 58962-004 Vamousse Lice Protection

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 58962-004?
  4. Vamousse Lice Protection 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:
58962-004
Proprietary Name:
Vamousse Lice Protection
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tyratech, Inc.
Labeler Code:
58962
Product Label ID:
084e1f03-3ce0-4663-b98b-74516ee9fc43
Start Marketing Date: [9]
04-29-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 58962-004?

The NDC code 58962-004 is assigned by the FDA to the product Vamousse Lice Protection which is product labeled by Tyratech, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58962-004-01 1 bottle, plastic in 1 carton / 236 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.

What are the uses for Vamousse Lice Protection?

Adults and children 2 years and older:Apply a generous amount of shampoo to wet hair, work into a lather and massage into scalp. Leave shampoo in hair for at least 3 minutes. Rinse.For protection against a head lice infestation, use daily for at least 10 to 14 days to kill any lice that may have hatched.For an active head lice infestation, use Vamousse® Lice Treatment before using this shampoo.Children under 2 years: ask a doctor.Product may be used as often as needed.

Which are Vamousse Lice Protection UNII Codes?

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

Which are Vamousse Lice Protection 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".