NDC 47219-342 Luxury Feet

Naja Naja Venom

NDC Product Code 47219-342

NDC 47219-342-02

Package Description: 1 BOTTLE, WITH APPLICATOR in 1 BOX > 60 mL in 1 BOTTLE, WITH APPLICATOR

NDC Product Information

Luxury Feet with NDC 47219-342 is a a human over the counter drug product labeled by Nutra Pharma Corporation. The generic name of Luxury Feet is naja naja venom. The product's dosage form is gel and is administered via topical form.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Luxury Feet Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Nutra Pharma Corporation
Labeler Code: 47219
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 07-15-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Luxury Feet Product Label Images

Luxury Feet Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Asian Cobra Venom 4x




*According to the Homeopathic Pharmacopeia of the United States


Temporarily relieves joint pain associated with overuse and pain associated with arthritis.


- For external use only.- If pain persist, consult a physician.- Avoid contact with eyes. - Pregnant or nursing women and children should consult a physician before use

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children

Directions For Use:

  • Remove protective wrapping
  • Liberally apply gel to the affected area and rub into joints.Use 3-4 time per day for the first week. Use as needed thereafter to relieve discomfort.Allow several days for drug to take maximum effect.

Other Information:

  • Do not use if container seal is broken prior to opening.
  • This product is intended for use in cases of recurring joint pain.This product is NOT intended to treat disease, it provides a temporary level of comfort, relief and a feeling of wellness.
  • This product has been determined to be safe and effective for moderate to sever (Stage 2) chronic pain, as indicated by the Homeopathic Pharmacopeia of the United States.

Otc - Ask Doctor

  • Pregnant or nursing women and children should consult a physician before use.

Inactive Ingredients:

Benzalkonium chloride, Ethanol, Methocel, Propylene glycol, Saline.

Otc - Questions

For more information visit: www.Nyloxin.comManufactured for Nutra Pharma1537 NW 65th Avenue

Plantation, FL 33313

Questions? (954) 834-3740

* Please review the disclaimer below.