Coconut Cosmetics 3-in-1 Serum

Anti-aging, Anti-fungal, Anti-acne Coconut Serum


Fiesta Ingredients Spain Sociedad Limitada
Human Otc Drug
NDC 82731-001
Coconut Cosmetics 3-in-1 Serum also known as Anti-aging, Anti-fungal, Anti-acne Coconut Serum is a human otc drug labeled by 'Fiesta Ingredients Spain Sociedad Limitada'. National Drug Code (NDC) number for Coconut Cosmetics 3-in-1 Serum is 82731-001. This drug is available in dosage form of Oil. The names of the active, medicinal ingredients in Coconut Cosmetics 3-in-1 Serum drug includes Cocoa Butter - 19.996 g/20mL . The currest status of Coconut Cosmetics 3-in-1 Serum drug is Active.

Drug Information:

Drug NDC: 82731-001
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: Coconut Cosmetics 3-in-1 Serum
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: Anti-aging, Anti-fungal, Anti-acne Coconut Serum
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Fiesta Ingredients Spain Sociedad Limitada
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Oil
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:COCOA BUTTER - 19.996 g/20mL
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: OTC MONOGRAPH FINAL
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: 15 May, 2022
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 23 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.
Application Number: part347
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
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:Fiesta Ingredients Spain Sociedad Limitada
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:512OYT1CRR
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
82731-001-0120 mL in 1 CARTON (82731-001-01)15 May, 2022N/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:

Designed to nourish facial skin as an anti-aging serum. purpose

Product Elements:

Coconut cosmetics 3-in-1 serum anti-aging, anti-fungal, anti-acne coconut serum lavender oil rosemary oil coconut oil cocoa butter cocoa butter lemon oil

Indications and Usage:

Apply a few drops after showering. usage

Warnings:

Https://www.coconutcosmetics.es/prospectus/ generally it is safe for any skin type if used in moderation. but check and observe for any alergic reactions before use and if there is any, stop using it. some studies claim that coconut oil is not recommended for oily skin because of its blocking-of-pores tendency. we dispute this claim because coconut oil, and especially our formulation, if applied according to our recommended method in this prospectus (application after showering and exfoliating with a hot towel), can aide in the function of human sebum (the cause of oily skin) but without the blockage of pores.

Dosage and Administration:

Instructions for use apply a drop of this size o daily on the affected skin and massage the area around. instructions for use

Package Label Principal Display Panel:

Outer packaging label


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.