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NDC 10893-840 Naturasil Molluscalm Treatment Kit

Sulfur,Thuja Occidentalis Kit - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 10893-840?
  5. Naturasil Molluscalm Treatment Kit Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
10893-840
Proprietary Name:
Naturasil Molluscalm Treatment Kit
Non-Proprietary Name: [1]
Sulfur, Thuja Occidentalis
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Nature's Innovation, Inc.
Labeler Code:
10893
Product Label ID:
20d254fe-718c-4fd4-b56a-e891257de311
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
08-21-2023
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)

Code Structure Chart

Product Details

What is NDC 10893-840?

The NDC code 10893-840 is assigned by the FDA to the product Naturasil Molluscalm Treatment Kit which is a human over the counter drug product labeled by Nature's Innovation, Inc.. The generic name of Naturasil Molluscalm Treatment Kit is sulfur, thuja occidentalis. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 10893-840-02 1 kit in 1 kit * 15 ml in 1 bottle (10893-810-15) * 118.3 g in 1 box (10893-830-04). 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 Naturasil Molluscalm Treatment Kit?

Thoroughly wash and dry area. Apply 3-4 times daily to affected area. Bumps will diminish and flake away over 2-6 weeks depending on severity of condition. Some individuals may be sensitive to essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use. Use soap at least 2 times per day, for 4-10 days. Drying of skin may occur. Some individuals may be sensitive to essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

Which are Naturasil Molluscalm Treatment Kit UNII Codes?

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

Which are Naturasil Molluscalm Treatment Kit 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.

[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.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".