Itsrt Tea Tree Oil And Argan Oil
NDC 84751-097

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 84751-097?
  5. Itsrt Tea Tree Oil And Argan Oil 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 inactivated by the FDA.

Itsrt Tea Tree Oil And Argan Oil is a OTC MONOGRAPH DRUG-approved product labeled by Guangzhou Qiaoyangzi Cosmetics 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 84751-097 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
84751-097
Proprietary Name:
Itsrt Tea Tree Oil And Argan Oil
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Guangzhou Qiaoyangzi Cosmetics Technology Co Ltd
Labeler Code:
84751
Product Label ID:
299b15a0-4e00-776b-e063-6294a90a03df
FDA Application Number: [6]
M032
Marketing Category: [8]
OTC MONOGRAPH DRUG

Marketing Timeline

Start Marketing Date: [9]
10-01-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
I

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 84751-097?

The NDC code 84751-097 is assigned by the FDA to the product Itsrt Tea Tree Oil And Argan Oil. This pharmaceutical product is labeled by Guangzhou Qiaoyangzi Cosmetics 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: 84751-097-01. 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?

This product is used as Purpose: Cleansing: Removes dirt, oil, and buildup from hair and scalp. Moisturizing: Helps to hydrate and retain moisture in hair. Soothing: Relieves scalp irritation and discomfort. Antioxidant Protection: Provides protection against environmental damage. Promotes Hair Health: Strengthens and nourishes hair to promote healthy growth. Exfoliation: Helps to gently exfoliate the scalp to reduce flakiness and buildup. . Indications & Usage: This shampoo is indicated for: Cleansing the hair and scalp: Effectively removes dirt, excess oil, and product buildup. Moisturizing and hydrating: Helps maintain the moisture balance of the hair and scalp, leaving hair soft and nourished. Soothe irritated or sensitive scalps: Soothes the scalp to reduce itching, dryness, and inflammation. Promoting hair health: Strengthens hair, supports healthy growth, and helps reduce hair breakage. Preventing and treating dandruff: Gently exfoliates the scalp to remove dead skin cells, reducing flakiness and preventing dandruff. Providing antioxidant protection: Protects the scalp and hair from damage caused by environmental stressors.

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 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".