EQUINE PAIN AWAY- naja naja venom gel 
Nutra Pharma Corporation

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Active Ingredients

Asian Cobra Venom 4x (30 mcg/mL)

Purpose

Analgesic*
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*According to the Homeopathic Pharmacopeia of the United States

Uses:

Temporarily relieves pain associated with arthritis, inflamed joints and overuse in horses.

Warnings:

Directions for Use:

• Remove protective wrapping.
• Liberally apply gel to the affected area and rub into joints.
• Use 1-2 times 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 tamper-proof tab is broken.
• This product is NOT intended to treat disease, it can provide a temporary level of comfort, relief and a feeling of wellness.
• This product has been determined to be safe and effective for moderate to severe chronic pain, as indicated by the Homeopathic Pharmacopeia     of the United States.

• Clinical experience suggests Equine Pain-Away may provide relief from other forms of pain.

Inactive Ingredients:

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

For more information visit: www.Nyloxin.com

Manufactured by NutraPharma

1537 NW 65th Avenue

Plantation, FL 33313

Questions? (954) 834-3740

Product label

image description

EQUINE PAIN AWAY 
naja naja venom gel
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:47219-242
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 (1600000 WAMW) (UNII: RFW2ET671P)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47219-242-081 in 1 BOX
1235 mL in 1 BOTTLE, DISPENSING
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/15/2021
Labeler - Nutra Pharma Corporation (141236286)
Establishment
NameAddressID/FEIBusiness Operations
Nutra Pharma Corporation141236286manufacture, api manufacture

Revised: 11/2022
Document Id: 37c55389-4007-4487-8ac6-06d4dbc39e6f
Set id: 37f28ef8-ab00-4924-ac59-58b2adc931b4
Version: 3
Effective Time: 20221129
 
Nutra Pharma Corporation