Naturasil Molluscum Treatment Kit
Thuja Occidentalis, Sulfur
Nature's Innovation, Inc.
Human Otc Drug
NDC 10893-510Naturasil Molluscum Treatment Kit also known as Thuja Occidentalis, Sulfur is a human otc drug labeled by 'Nature's Innovation, Inc.'. National Drug Code (NDC) number for Naturasil Molluscum Treatment Kit is 10893-510. This drug is available in dosage form of Kit. The names of the active, medicinal ingredients in Naturasil Molluscum Treatment Kit drug includes . The currest status of Naturasil Molluscum Treatment Kit drug is Active.
Drug Information:
| Drug NDC: | 10893-510 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Naturasil Molluscum Treatment Kit |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Thuja Occidentalis, Sulfur |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Nature's Innovation, Inc. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Kit |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | |
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 19 Oct, 2021 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 12 Jun, 2026 |
| 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. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Nature's Innovation, Inc.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | |
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 10893-510-02 | 1 KIT in 1 KIT (10893-510-02) * 15 mL in 1 BOTTLE, GLASS (10893-500-15) * 113.3 g in 1 CARTON (10893-610-04) | 19 Oct, 2021 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose polypi and naevi symptom relief
Purpose: molluscum contagiosum symptom relief.
Product Elements:
Naturasil molluscum treatment kit thuja occidentalis, sulfur naturasil molluscum thuja occidentalis thuja occidentalis leafy twig thuja occidentalis leafy twig cedar leaf oil tea tree oil castor oil naturasil molluscum relief sulfur, thuja occindentalis sulfur sulfur thuja occidentalis leaf thuja occidentalis leaf water citric acid monohydrate cocamidopropyl betaine coconut oil glycerin glyceryl laurate lavender oil pentasodium pentetate propylene glycol sodium chloride sodium citrate, unspecified form sodium laurate sodium myristate sodium oleate sodium stearate sodium thiosulfate sorbitol etidronate tetrasodium titanium dioxide trisodium sulfosuccinate
Indications and Usage:
Uses: symptomatic treatment of molluscum contagiosum.
Uses: symptomatic homeopathic topical treatment of common molluscum contagiosum.
Warnings:
Warnings: for external use only. ask a doctor before use if pregnant or nursing. avoid using near eyes or mouth. keep out of reach of children. do not use if tamper evident seal is broken. in case of ingestion call poison control center hotline immediately at 1-800-222-1222.
Warnings: for external use only. ask a doctor before use if pregnant or nursing. avoid using near eyes, mouth or mucous membranes. if contact with eyes or mucous membranes occurs, rinse thoroughly with water. keep out of reach of children. in case of ingestion, call poison control center hotline immediately at 1-800-222-1222
Dosage and Administration:
Directions: thoroughly wash and dry area. apply 3-4 times daily to affected area. molluscum 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.
âdirections: 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.
Package Label Principal Display Panel:
Packaging kit component kit
Further Questions:
Questions? comments? (866)-371-2499 www.naturasil.com mfd. by: nature's innovation, inc. 5317 palmero court, buford, ga 30518 ⢠made in the u.s.a. not tested on animals. nmtk r2-102121
Questions? comments? (866)371-2499 ⢠www.naturasil.com mfd. by: natureâs innovation, inc. 5317 palmero court, buford, ga 30518 made in the u.s.a. not tested on animals.