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  4. NDC Product Code: 84751-095 Itsrt Tea Tree Oil And Argan Oil

NDC 84751-095 Itsrt Tea Tree Oil And Argan Oil

Liquid Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 84751-095?
  5. Itsrt Tea Tree Oil And Argan Oil Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 84751-095 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:
84751-095
Proprietary Name:
Itsrt Tea Tree Oil And Argan Oil
Non-Proprietary Name: [1]
Itsrt Tea Tree Oil And Argan Oil
Substance Name: [2]
Aloe Vera Leaf; Biotin; Caffeine; Fallopia Multiflora Root; Glycerin; Green Tea Leaf; Panthenol; Rosemary; Salicylic Acid; Selenium Sulfide
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Labeler Name: [5]
Guangzhou Qiaoyangzi Cosmetics Technology Co Ltd
Labeler Code:
84751
Product Label ID:
25b046bb-6ee4-bebc-e063-6394a90aec6a
FDA Application Number: [6]
M016
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
10-01-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 84751-095?

The NDC code 84751-095 is assigned by the FDA to the product Itsrt Tea Tree Oil And Argan Oil which is a human over the counter drug product labeled by Guangzhou Qiaoyangzi Cosmetics Technology Co Ltd. The product's dosage form is liquid and is administered via topical form. The product is distributed in a single package with assigned NDC code 84751-095-01 500 ml in 1 bottle, pump . 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 Itsrt Tea Tree Oil And Argan Oil?

This product is used as ShampooHair CareBody Wash / BathingDandruff ControlHair Loss PreventionFragrance. Directions Shampoo usage instructions Wet hair or body.Pour out an appropriate amount of shampoo and rubit with your palm to create bubbles.Apply the product to hair or gently rub on the body fora few minutes to ensure even coverage. Rinse hair and body with running warm water, do notrub vigorously. The water temperature should not betoo high to prevent hair from losing its luster. Simplyrinse it off thoroughly. If necessary, repeat the above steps for shampooingFinally, gently pinch dry hair with your hands or wipehair and body with a dry towel.

What are Itsrt Tea Tree Oil And Argan Oil Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • ALOE VERA LEAF 1 mg/500mL
  • BIOTIN .01 mg/500mL - A water-soluble, enzyme co-factor present in minute amounts in every living cell. It occurs mainly bound to proteins or polypeptides and is abundant in liver, kidney, pancreas, yeast, and milk.
  • CAFFEINE .1 mg/500mL - A methylxanthine naturally occurring in some beverages and also used as a pharmacological agent. Caffeine's most notable pharmacological effect is as a central nervous system stimulant, increasing alertness and producing agitation. It also relaxes SMOOTH MUSCLE, stimulates CARDIAC MUSCLE, stimulates DIURESIS, and appears to be useful in the treatment of some types of headache. Several cellular actions of caffeine have been observed, but it is not entirely clear how each contributes to its pharmacological profile. Among the most important are inhibition of cyclic nucleotide PHOSPHODIESTERASES, antagonism of ADENOSINE RECEPTORS, and modulation of intracellular calcium handling.
  • FALLOPIA MULTIFLORA ROOT .15 mg/500mL
  • GLYCERIN 1.5 mg/500mL
  • GREEN TEA LEAF .1 mg/500mL
  • PANTHENOL .5 mg/500mL
  • ROSEMARY .09 mg/500mL
  • SALICYLIC ACID .1 mg/500mL - A compound obtained from the bark of the white willow and wintergreen leaves. It has bacteriostatic, fungicidal, and keratolytic actions.
  • SELENIUM SULFIDE .5 mg/500mL

Which are Itsrt Tea Tree Oil And Argan Oil UNII Codes?

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

Which are Itsrt Tea Tree Oil And Argan Oil 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

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[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.

[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".