NYLOXIN- naja naja venom gel 
Nutra Pharma Corporation

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Nyloxin Topical Gel ES

Active Ingredients

Asian Cobra Venom 4x

Purpose

Analgesic*
___________________________________________________________

*According to the Homeopathic Pharmacopeia of the United States

Uses:

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

Warnings:

- For external use only.

- If symptoms persist or worsen, discontinue use and seek medical attention.

- Avoid contact with eyes. If product gets into eyes flush with water. Seek Medical attention.

- Not for use on open wounds.


Keep out of the reach of children

Directions for Use:

Other Information:

Inactive Ingredients:

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

For more information visit: www.Nyloxin.com

Manufactured for Nutra Pharma

1537 NW 65th Avenue

Plantation, FL 33313

Product label

image description

image description

NYLOXIN 
naja naja venom gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47219-311
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM) NAJA NAJA VENOM4 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
ALCOHOL (UNII: 3K9958V90M)  
HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47219-311-021 in 1 BOX08/23/2010
160 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/23/2010
Labeler - Nutra Pharma Corporation (141236286)

Revised: 7/2021
Document Id: c71b3c68-d5d0-6e4f-e053-2a95a90ab98f
Set id: c28c50db-4b6b-4307-8fcb-9020d6ae9cd3
Version: 4
Effective Time: 20210714
 
Nutra Pharma Corporation