Lice Treatment Dedicated
NDC 87276-001

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 87276-001?
  5. Lice Treatment Dedicated Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

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

Lice Treatment Dedicated is a OTC MONOGRAPH DRUG-approved product labeled by Shenzhen Zhenshangzekai Technology Co., Ltd.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a white product. This product entry covers the primary NDC 87276-001 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
87276-001
Proprietary Name:
Lice Treatment Dedicated
Product Type: [3]
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Shenzhen Zhenshangzekai Technology Co., Ltd.
Labeler Code:
87276
Product Label ID:
459aafa5-08d4-3667-e063-6294a90a3b94
FDA Application Number: [6]
M031
Marketing Category: [8]
OTC MONOGRAPH DRUG

Marketing Timeline

Start Marketing Date: [9]
12-10-2025
End Marketing Date: [10]
08-06-2026
Listing Expiration Date: [11]
08-06-2026
Exclude Flag: [12]
D

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 87276-001?

The NDC code 87276-001 is assigned by the FDA to the product Lice Treatment Dedicated. This pharmaceutical product is labeled by Shenzhen Zhenshangzekai Technology Co., Ltd. and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 87276-001-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Directions Important: Read warnings before use .Children 6 months of age to under 12 years of age : an adult should supervise use Adults and children 6 months of age and over: Inspect All houschold members should be checked by anothe!person for lice and/or nits (eggs) Use a magnifying glassin bright light to help you see thelice and/or nits(eggs) Use a tool, such as a comb or two unsharpened pencilsto lift and part the hair Look for tiny nits near the scalp, beginning at the backof theneck and behind the ears Examine small sections ofthe hair (1-2 inches wide) ata time .Unlike dandruff, nits stick to the hair, Dandruff shouldmove when lightly touched If either lice or nits (eggs) are found, treat with product Treat Your hair and scalp must be DRY before applyingproduct Apply the product directly onto dry hair and scalp Completely cover your scalp and hair closest to thescalp first.and then apply outwards towards the endsofyour hair Use only as much asneeded to fully cover hair andscalp up to one full bottle, and discard the remainingRub product throughout your hair Itis important to completely cover your entire head sothat all lice and eggs are exposed to the lotion, Be surethat each hair is coated from the scalp to the tip Wait and Rinse Allow product to stay on your hair and scalp for 10minutes after it has been applied, Use a timer or clockStart timing after you have completely covered yourhair and scalp with product. After 10 minutes, rinse product completely from youhair and scalp using only water. After rinsing, dry and style hair as usual. Wait 24 hoursbefore applying shampoo. After treatmentWash your hands after applying product. -Nit combing is not necessary whentreating with product for it to work, but ifdesired, a fne-tooth comb or special nitcomb may be used to remove dead liceand nits.This is a single use product, Discard bottle after use.Do not use again on the same personand same lice infestation without talkingto a healthcare provider frst.If infestation continues, see a doctor forother treatments. Machine wash any bedding and clothingused by anyone having lice, Machinewash at high temperatures (150°F) andtumble in a hot dryer for 20 minutes.After fnishing treatment with licemedicine, check everyone in your famillyfor lice after one week. Considertreatment for those who have lice.

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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.
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".