NDC 58962-003 Vamousse Lice Prevention

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:
58962-003
Proprietary Name:
Vamousse Lice Prevention
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tyratech, Inc.
Labeler Code:
58962
Start Marketing Date: [9]
01-16-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 58962-003-01

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 236 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 58962-003?

The NDC code 58962-003 is assigned by the FDA to the product Vamousse Lice Prevention 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 58962-003-01 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 Prevention?

Important: Read Warnings before use. Adults and children 6 months and over:Apply a generous amount of shampoo to wet hair, work into a lather and massage into scalp. Rinse thoroughly.Repeat process and leave shampoo on hair for at least 3 minutes.To treat head lice infestation, use the shampoo daily for at least 2 weeks.For best results on an extreme head lice infestation, use Vamousse treatment before using shampoo.Product may be used as often as needed.

Which are Vamousse Lice Prevention UNII Codes?

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

Which are Vamousse Lice Prevention 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".