Shailee Tea Tree Body Wash Liquid
NDC 84938-009

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 84938-009?
  4. Shailee Tea Tree Body Wash Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

Shailee Tea Tree Body Wash (thyme oil,melaleuca alternifolia,oregano oil,lavender oi,undecylenic acidl) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Foshan Sugar Max Cosmetics Co.,ltd. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a liquid for topical administration. This product entry covers the primary NDC 84938-009 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
84938-009
Proprietary Name:
Shailee Tea Tree Body Wash
Non-Proprietary Name: [1]
Thyme Oil, Melaleuca Alternifolia, Oregano Oil, Lavender Oi, Undecylenic Acidl
Substance Name: [2]
Lavender Oil; Oregano Leaf Oil; Tea Tree Oil; Thyme Oil; Undecylenic Acid
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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 & Regulatory Data

Labeler Name: [5]
Foshan Sugar Max Cosmetics Co.,ltd
Labeler Code:
84938
Product Label ID:
3930ab37-9d6a-424e-9eac-a55283afc303
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
10-30-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 84938-009?

The NDC code 84938-009 is assigned by the FDA to the product Shailee Tea Tree Body Wash. It is commonly known by its generic name, thyme oil, melaleuca alternifolia, oregano oil, lavender oi, undecylenic acidl. This pharmaceutical product is labeled by Foshan Sugar Max Cosmetics Co.,ltd and is currently categorized as listed product. The medication is a liquid administered via topical route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 84938-009-01. 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 Tea Tree Oil (Melaleuca alternifolia) 6X HPx                  Antifungal treatmentThyme Oil (Thymus vulgaris) – 6X HPx                        Antifungal treatmentOregano Oil   6X HPx                                                Antifungal treatmentLavender Oil (Lavandula angustifolia)  4X HPx            Antifungal treatmentUndecylenic Acid    10X HPx                                       Antifungal treatment. For the treatment of most ● jock itch (tinea cruris) ● ringworm (tinea corporis) ● athlete's foot (tinea pedis) ● tinea versicolor For relief of: ● itching ● scaling ● cracking ● burning ● irritation

What are Active Ingredients of this product?

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.

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 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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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".