Toenail Fungus / Nail Repair Pen
Tea Tree Oil
Vital Synergy Llc
Human Otc Drug
NDC 82743-101Toenail Fungus / Nail Repair Pen also known as Tea Tree Oil is a human otc drug labeled by 'Vital Synergy Llc'. National Drug Code (NDC) number for Toenail Fungus / Nail Repair Pen is 82743-101. This drug is available in dosage form of Solution. The names of the active, medicinal ingredients in Toenail Fungus / Nail Repair Pen drug includes Tea Tree Oil - 10 [hp_X]/100mL . The currest status of Toenail Fungus / Nail Repair Pen drug is Active.
Drug Information:
| Drug NDC: | 82743-101 |
| 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: | Toenail Fungus / Nail Repair Pen |
| 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: | Tea Tree Oil |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Vital Synergy Llc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Solution |
| 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: | TEA TREE OIL - 10 [hp_X]/100mL
|
| 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: | 16 May, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 19 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: | VITAL SYNERGY LLC
|
| 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: | VIF565UC2G
|
| 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 |
|---|
| 82743-101-30 | 1 BOTTLE, WITH APPLICATOR in 1 BOX (82743-101-30) / 30 mL in 1 BOTTLE, WITH APPLICATOR (82743-101-01) | 16 May, 2022 | N/A | No |
| 82743-101-63 | 6 BOTTLE, WITH APPLICATOR in 1 BOX (82743-101-63) / 3 mL in 1 BOTTLE, WITH APPLICATOR (82743-101-03) | 16 May, 2022 | 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 antifungal
Product Elements:
Toenail fungus / nail repair pen tea tree oil tea tree oil tea tree oil almond oil tocopherol aloe vera whole ascorbic acid eucalyptus oil lavender oil
Indications and Usage:
Uses strong nails fast yellow broken brittle toenails & fingernails
Warnings:
Warnings for external use only. avoid contact with eyes. discontinue use if adverse skin reaction occurs. consult your health care physician if pregnant, nursing, or for a child under the age of two.
Dosage and Administration:
Directions test on a small part of a nail first. apply topically twice per day on the affected area.
Package Label Principal Display Panel:
01b uc_vital synergy_nail repair pen_3ml 01b uc_vital synergy_toenail fungus solution_30ml