Naturasil Jock Itch
Sulfur
Nature's Innovation, Inc.
Human Otc Drug
NDC 10893-200Naturasil Jock Itch also known as Sulfur is a human otc drug labeled by 'Nature's Innovation, Inc.'. National Drug Code (NDC) number for Naturasil Jock Itch is 10893-200. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Naturasil Jock Itch drug includes Sulfur - 6 [hp_X]/1 . The currest status of Naturasil Jock Itch drug is Active.
Drug Information:
| Drug NDC: | 10893-200 |
| 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 Jock Itch |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Proprietary Name Base: | Naturasil |
| The base of the Brand/Proprietary name excluding its suffix. |
| Proprietary Name Suffix: | Jock Itch |
| A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard. |
| 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: | 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: | Liquid |
| 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: | SULFUR - 6 [hp_X]/1
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| 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: | 02 Feb, 2012 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 15 Jan, 2025 |
| 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: | 70FD1KFU70
|
| 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 |
|---|
| 10893-200-15 | 1 LIQUID in 1 BOTTLE, GLASS (10893-200-15) | 02 Feb, 2012 | 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 jock itch symptom relief
Product Elements:
Naturasil jock itch sulfur sulfur sulfur west indian lemongrass oil eucalyptus oil jojoba oil lavender oil tea tree oil patchouli oil
Indications and Usage:
Uses uses: symptomatic treatment of jock itch (tinea cruris).
Warnings:
Warnings warnings: for external use only. ask a doctor before use if pregnant or nursing. avoid using near eyes, mouth or mucous membranes. 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.
Do Not Use:
Warnings warnings: for external use only. ask a doctor before use if pregnant or nursing. avoid using near eyes, mouth or mucous membranes. 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.
Dosage and Administration:
Directions directions: apply 3 times per day to affected area until jock itch has cleared. to speed healing, we recommend naturasil sulfur lavender soap. some individuals may be sensitive to essential oils. skin test for tolerability. if irritation or reaction occurs, discontinue use.
Description:
The letters hpus indicate the component(s) in this product is (are) officially monographed in the homeopathic pharmacopeia of the united states.
Package Label Principal Display Panel:
100% natural plant extracts naturasil ml (fl. oz.) topical liquid homeopathic medicine jock itch 15 ml label
Further Questions:
Questions questions? comments? www.naturasil.com 1-866-371-2499 mfd. by: nature's innovation, inc., 2723 brickton north dr., buford, ga 30518 not tested on animals.