NDC 0363-0955 Lice Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Get all the details for National Drug Code (NDC) 0363-0955 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
0363-0955
Proprietary Name:
Lice Treatment
Product Type: [3]
Labeler Name: [5]
Labeler Code:
0363
FDA Application Number: [6]
ANDA076090
Marketing Category: [8]
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date: [9]
07-15-2010
End Marketing Date: [10]
03-01-2025
Listing Expiration Date: [11]
03-01-2025
Exclude Flag: [12]
D
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Product Details

What is NDC 0363-0955?

The NDC code 0363-0955 is assigned by the FDA to the product Lice Treatment which is product labeled by Walgreen Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-0955-26 2 bottle in 1 carton / 59 ml in 1 bottle. 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 Lice Treatment?

Inspect•all household members should be checked by another person for lice and/or nits (eggs)•use a magnifying glass in bright light to help you see the lice and nits (eggs)•use a tool, such as a comb or two unsharpened pencils to lift and part the hair•look for tiny nits near the scalp, beginning at the back of the neck and behind the ears•small sections of hair (1-2 inches wide) should be examined at a time•unlike dandruff, nits stick to the hair. Dandruff should move when lightly touched.•if either lice or nits (eggs) are found, treat with the creme rinseTreat•wash hair with a shampoo without conditioner. Do not use a shampoo that contains a conditioner or a conditioner alone since this may decrease the activity of the creme rinse. Rinse with water.•towel dry hair so it is damp but not wet•shake the bottle well•completely saturate the hair and scalp with the creme rinse. Begin to apply the creme rinse behind the ears and at the back of the neck.•keep the creme rinse out of the eyes. Protect the eyes with a washcloth or towel.•leave the creme rinse on the hair for 10 minutes, but no longer•rinse with warm water•towel dry hair and comb out tangles•if live lice are seen seven days or more after the first treatment, a second treatment should be givenRemove Lice/Nits•remove nits by combing the hair with the special small tooth comb provided. Remaining nits may be removed by hand (using a throw-away glove), or cutting the nits out.•use the nit comb provided and make sure the hair remains slightly damp while removing nits•if the hair dries during combing, dampen it slightly with water•part the hair into 4 sections. Work on one section at a time. Longer hair may take more time (1-2 hours).•start at the top of the head on the section you have picked•with one hand, lift a 1-2 inch wide strand of hair. Get the teeth of the comb as close to the scalp as possible and comb with a firm, even motion away from the scalp to the end of the hair.•use clips to pin back each strand of hair after you have combed out the nits•clean the comb completely as you go. Wipe the nits from the comb with a tissue and throw away the tissue in a sealed plastic bag to prevent the lice from coming back.•after combing, recheck the entire head for nits and repeat combing if necessary•check the affected head daily to remove any nits that you might have missed

Which are Lice Treatment UNII Codes?

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

Which are Lice Treatment 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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Patient Education

Permethrin Topical


Permethrin is used to treat scabies ('mites that attach themselves to the skin) in adults and children 2 months of age and older. Over-the-counter permethrin is used to treat lice (small insects that attach themselves to the skin on the head) in adults and children 2 months of age and older. Permethrin is in a class of medications called scabicides and pediculicides. It works by killing lice and mites.
[Learn More]


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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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".