FDA.reportPublic FDA data

Luxury feet

Manufacturer
Nutra Pharma Corporation
Effective date
2021-07-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:14:43

Label at a glance#

ProductLuxury feet
Active ingredientNAJA NAJA VENOM
Label structure11 sections

Indications and uses

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

Dosage and administration

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.

Storage and handling

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.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Asian Cobra Venom 4x 

Purpose

OTC - PURPOSE SECTION

Analgesic*
___________________________________________________________

*According to the Homeopathic Pharmacopeia of the United States

Uses:

INDICATIONS & USAGE SECTION

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

Warnings:

WARNINGS SECTION

- 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 SECTION

Keep out of the reach of children

Directions for Use:

DOSAGE & ADMINISTRATION SECTION

  • 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:

STORAGE AND HANDLING SECTION

  • 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 SECTION

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

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

For more information visit: www.Nyloxin.com

Manufactured for Nutra Pharma

1537 NW 65th Avenue
Plantation, FL 33313

Questions? 

(954) 834-3740

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47219-342-022024-01-30C16284748780-11030e365-00d3-111a-e063-dadaa90a10e23eec14d2-45a8-4ae5-abd8-65943a0712ac

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47219-342-02Luxury feet60 mL in 1 BOTTLE, WITH APPLICATORGEL601
47219-342-02Luxury feet1 in 1 BOXGEL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47219-342LUXURY FEET (NAJA NAJA VENOM) GEL [NUTRA PHARMA CORPORATION]1Legacy NDC, 2 package rows20210717_3eec14d2-45a8-4ae5-abd8-65943a0712ac.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47219-34247219-342-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
ALCOHOL3K9958V90MIACT
HYDROXYPROPYL CELLULOSE (1600000 WAMW)RFW2ET671PIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM CHLORIDE451W47IQ8XIACT
NAJA NAJA VENOMZZ4AG7L7VMACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c730bb13-e53e-c008-e053-2995a90a771b3eec14d2-45a8-4ae5-abd8-65943a0712ac2021-07-15WarningsExact identifier
spl id: c730bb13-e53e-c008-e053-2995a90a771b
spl set id: 3eec14d2-45a8-4ae5-abd8-65943a0712ac

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.