NDC 30807-3003 Quit Nits Preventative

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:
30807-3003
Proprietary Name:
Quit Nits Preventative
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 30807-3003?

The NDC code 30807-3003 is assigned by the FDA to the product Quit Nits Preventative 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 30807-3003-4 1 bottle, spray in 1 box / 125 ml in 1 bottle, spray. 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 Preventative?

ApplyOn the day following the lice treatment lightly spray Quit Nits Preventative onto dry hair until the hair is dampCombUse a regular comb or brush to distribute Quit Nits Preventative evenly throughout the hairRepeatFor best results, repeat daily or before children play with untreated children

Which are Quit Nits Preventative UNII Codes?

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

  • EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
  • EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (Active Moiety)

Which are Quit Nits Preventative 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".