NDC 30807-2002 Quit Nits Advance

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:
30807-2002
Proprietary Name:
Quit Nits Advance
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
30807
Start Marketing Date: [9]
01-01-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 30807-2002?

The NDC code 30807-2002 is assigned by the FDA to the product Quit Nits Advance which is product labeled by Wild Child W A Pty Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 30807-2002-2 60 ml in 1 tube . 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 Quit Nits Advance?

Important: Read warnings and full directions. For more information read the enclosed Consumer Information Leaflet.For adults and children 6 months and over.APPLYapply the entire contents of one tube thoroughly to dry hair, starting from behind the ears to the back of the neck, working forward.to be effective, all lice and eggs must come in contact with product, ensure hair and scalp are saturated. For long or very thick hair two tubes may be required.COVERuse the shower cap supplied to keep hair damp, leave on for 4 hours before washing.for serious infestation remove shower cap after 4 hours and leave product on overnight.WASHwash area thoroughly with warm water and regular shampoo. Towel hair dry and comb out tangles using a regular comb or brush.as an option remove any remaining lice or nits with the included nit comb or fingernails.if hair dries during combing dampen slightly with water.

Which are Quit Nits Advance UNII Codes?

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

Which are Quit Nits Advance 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".