Arnica Treatment Pack
Nartex Laboratorios Homeopaticos Sa De Cv
Human Otc Drug
NDC 34666-020Arnica Treatment Pack is a human otc drug labeled by 'Nartex Laboratorios Homeopaticos Sa De Cv'. National Drug Code (NDC) number for Arnica Treatment Pack is 34666-020. This drug is available in dosage form of Kit. The names of the active, medicinal ingredients in Arnica Treatment Pack drug includes . The currest status of Arnica Treatment Pack drug is Active.
Drug Information:
| Drug NDC: | 34666-020 |
| 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: | Arnica Treatment Pack |
| 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: | Arnica Treatment Pack |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Nartex Laboratorios Homeopaticos Sa De Cv |
| 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: | ORAL
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: | 11 Apr, 2019 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 09 May, 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: | Nartex Laboratorios Homeopaticos SA DE CV
|
| 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. |
| UPC: | 0844827001013
|
| UPC stands for Universal Product Code. |
| 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 |
|---|
| 34666-020-01 | 1 KIT in 1 KIT (34666-020-01) * 1 TABLET in 1 BOX | 11 Apr, 2019 | 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 arnica montana 6c hpus* .....anti-inflammatory
Purpose arnica montana tinc hpus*.......anti-inflammatory/pain relief hamamelis virginiana tinc hpus.....anti-inflammatory/pain relief
Product Elements:
Arnica treatment pack arnica treatment pack arnica recovery arnica recovery tablets arnica montana arnica montana lactose, unspecified form starch, potato talc gelatin magnesium stearate none white (tablet) arnica recovery arnica recovery cream water petrolatum glycerin paraffin sodium benzoate lanolin arnica montana arnica montana hamamelis virginiana leaf hamamelis virginiana leaf
Indications and Usage:
Uses for the temporary relief of sore muscles, bruises, sprains product uses are based on homeopathic materia medica not clinical tests. this product has not been clinically tested by nartex labs usa, inc.
Warnings:
Warnings do not use if you have an allergy or hypersensitivity to the components of the fourmal or have had a prior reaction to this product.
Warnings for external use only. do not apply to wounds tor damaged skin apply over large areas of the body
When Using:
When using this product avoid contact with eyes or mucous membranes do not bandage tightly
Dosage and Administration:
Directions adults and children 4 yers of age and older: take 2 tablets every 6 hours, slowly dissolving in the mouth children under 4 years of age: consult a physician
Directions adults and children over 2 years of age: apply generously rubbing into affected area as needed children 2 years of age: consult a physcian
Stop Use:
Stop use and ask a doctor if symptoms persist for more than 7 das or clear up and occur again within a few days rash develops
Spl Patient Package Insert:
Drug facts
Package Label Principal Display Panel:
Principal display panel homeopathic arnica nartex for sore muscles and bruises homeopathic temporary relief for the symptoms of sore muscles, bruises, and sprains. combo pack there is no scientific evidence that the product works. product's claims are based only on theories of homeopathy from the 1700's that are not accepted by most modern medical experts. contains 1 tube net. wt. 1.05oz (29.7g) and 1 box 60 tablets arnica montana kit
Further Questions:
Questions or comments? informacion@nartexlabs.com or call 1-877-248-1970 between 9am and 5pm cst.
Questions or comments? informacion@nartexlabs.com or call 1-877-248-1970 between 9am and 5pm cst.