Curoxen Pain Relief

Olive Extract, Calendula, Arnica Montana


Organicare Nature's Science, Llc
Human Otc Drug
NDC 71042-002
Curoxen Pain Relief also known as Olive Extract, Calendula, Arnica Montana is a human otc drug labeled by 'Organicare Nature's Science, Llc'. National Drug Code (NDC) number for Curoxen Pain Relief is 71042-002. This drug is available in dosage form of Ointment. The names of the active, medicinal ingredients in Curoxen Pain Relief drug includes Arnica Montana - 3 [hp_X]/14g Calendula Officinalis Flowering Top - 3 [hp_X]/14g Olea Europaea Fruit Volatile Oil - 2 [hp_X]/14g . The currest status of Curoxen Pain Relief drug is Active.

Drug Information:

Drug NDC: 71042-002
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: Curoxen Pain Relief
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: Olive Extract, Calendula, Arnica Montana
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Organicare Nature's Science, Llc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Ointment
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:ARNICA MONTANA - 3 [hp_X]/14g
CALENDULA OFFICINALIS FLOWERING TOP - 3 [hp_X]/14g
OLEA EUROPAEA FRUIT VOLATILE OIL - 2 [hp_X]/14g
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: 24 Jan, 2017
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 25 Dec, 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, 2024
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:OrganiCare Nature's Science, 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:O80TY208ZW
18E7415PXQ
8E7358CX1J
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 NDCDescriptionMarketing Start DateMarketing End DateSample Available
71042-002-141 TUBE in 1 CARTON (71042-002-14) / 14 g in 1 TUBE24 Jan, 2017N/ANo
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 pain reliever healing agent antimicrobial and healing agent

Product Elements:

Curoxen pain relief olive extract, calendula, arnica montana lavender oil olive oil arnica montana arnica montana olea europaea fruit volatile oil olea europaea fruit volatile oil calendula officinalis flowering top calendula officinalis flowering top

Indications and Usage:

Use first aid to help prevent infection, promote healing, and relieve pain in minor: cuts scrapes burns

Warnings:

Warnings for external use only.

Do Not Use:

Warnings for external use only.

Dosage and Administration:

Directions clean the affected area apply a thin layer of curoxen to the affected area 3 times a day or as needed may be covered with a sterile bandage

Stop Use:

Stop use and ask a doctor if condition persists or gets worse rash or other allergic reaction develops

Package Label Principal Display Panel:

Curoxen® with arnica for pain relief first aid ointment a homeopathic medicine that helps prevent infection in minor cuts, scrapes, and burns net wt 0.5 oz (14.2 g) curoxen pain relief

Further Questions:

Questions? call 512-814-0038 or visit www.curoxen.com


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.