ULTIMATE PAIN BLOCK- naja naja venom spray, metered

Ultimate Pain Block by

Drug Labeling and Warnings

Ultimate Pain Block 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 4X

Purpose

Analgesic*

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

Inactive Ingredients:

Flavoring, Purified Water, Sodium benzoate, Sodium phosphate, Xylitol.

DIRECTIONS:

Gently pull down center tab.

Do not remove the tab. Open mouth.

Press pump four times directly into the mouth or under the tongue.

INDICATIONS & USAGE

USE SPRAY INITIALLY EVERY 3-4 HOURS.

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

KEEP OUT OF THE REACH OF CHILDREN

WARNINGS:

• For oral use only
• If pain persists, consult a physician
• Overuse may induce headaches

• 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.

Questions:

1-888-381-HEALTH

Principal Display Panel - 2 oz Bottle Label

PHYSICIAN'S
TOTAL HEALTH

ULTIMATE
PAIN BLOCK

PROFESSIONAL STRENGTH

CLINICALLY PROVEN LONG-LASTING
PAIN & INFLAMMATION RELIEF

Back Pain Neck Pain
Joint Pain Dental Pain
Migraines Neuralgia

ORAL SPRAY

HOMEOPATHIC

2OZ. NET WT.

INGREDIENTS AND APPEARANCE

ULTIMATE PAIN BLOCK 
naja naja venom spray, metered

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47219-215
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM)	NAJA NAJA VENOM	4 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM PHOSPHATE (UNII: SE337SVY37)
XYLITOL (UNII: VCQ006KQ1E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47219-215-01	1 in 1 BOX	10/29/2025
1		60 mL in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/29/2025

Labeler - Nutra Pharma Corporation (141236286)

Establishment
Name	Address	ID/FEI	Business Operations
Nutra Pharma Corporation		141236286	manufacture(47219-215) , api manufacture(47219-215)