PLUS RELIEF- naja naja venom gel

Plus Relief by

Drug Labeling and Warnings

Plus Relief by is a Homeopathic medication manufactured, distributed, or labeled by Nutra Pharma Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Asian Cobra Venom 6X

PURPOSE

Analgesic*

*Claims based on traditional Homeopathic practice not accepted medical evidence. Not FDA accepted.

Directions:

• Remove protective wrapping.
• Liberally apply gel to affected area.
• Rub thoroughly into hands and joints.

INDICATIONS & USAGE

USE 3-4 TIMES A DAY.

Note:It may take several days to induce relief. Use within 90 days of opening.
Store at 50° to 80°F.

Inactive Ingredients:

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

KEEP OUT OF THE REACH OF CHILDREN

WARNINGS:

• For external use only.
• If pain persists, consult a physician.
• Avoid contact with eyes. If product gets into eyes, flush with water. Seek medical attention.
• Not for use on open wounds.

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

Do not use if seal is broken prior to opening. This product is NOT intended to treat disease.

It provides a temporary level of comfort, relief and a feeling of wellness.

NDC: 47219-302-02

HOMEOPATHIC

Principal Display Panel - 2 oz Bottle Label

AVINIHEALTH ™
ADVANCES IN NATURAL HEALING

PLUS
RELIEF

Chronic Pain Relief

SUPER STRENGTH

TOPICAL GEL EASY SQUEEZE BOTTLE

Joint Pain ■ Neck Pain ■ Arthritis Pain
Pain from Repetitive Stress

2 oz. net wt.

INGREDIENTS AND APPEARANCE

PLUS RELIEF 
naja naja venom gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47219-302
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM)	NAJA NAJA VENOM	6 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
ALCOHOL (UNII: 3K9958V90M)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOTONIC SODIUM CHLORIDE SOLUTION (UNII: VR5Y7PDT5W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47219-302-02	1 in 1 BOX	10/27/2025
1		60 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/27/2025

Labeler - Nutra Pharma Corporation (141236286)

Establishment
Name	Address	ID/FEI	Business Operations
Nutra Pharma Corporation		141236286	manufacture(47219-302) , api manufacture(47219-302)